Medline ReNewal Reprocessed Boston Scientific Dynamic Tip Unidirectional Steerable Diagnostic Catheter

FDA 510(k) K252405 · Surgical Instrument Service and Savings, Inc.

Substantially Equivalent

510(k) numberK252405

Submission

Device name
Medline ReNewal Reprocessed Boston Scientific Dynamic Tip Unidirectional Steerable Diagnostic Catheter
Applicant
Surgical Instrument Service and Savings, Inc.
Redmond, OR, US
Received
July 31, 2025
Decision date
November 26, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NLH – Catheter, Recording, Electrode, Reprocessed
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1220
Specialty
Cardiovascular

Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

Other 510(k)s with product code NLH

510(k)DeviceApplicantDecision
K250772Medline ReNewal Reprocessed Boston Scientific Dynamic XT Unidirectional Steerable…NLH · Traditional Surgical Instrument Service and Savings, Inc.07/11/2025SE
K242225Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic CatheterNLH · Traditional Surgical Instrument Service and Savings, Inc.11/29/2024SE
K241224Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer…NLH · Traditional Surgical Instrument Service and Savings Inc.(Dba…11/15/2024SE
K240826Reprocessed DECANAV™ Electrophysiology Catheter; Reprocessed WEBSTER® Duo-Decapolar…NLH · Traditional Sterilmed, Inc.10/11/2024SE
K241156Medline ReNewal Reprocessed St. Jude Medical Response Electrophysiology Catheter…NLH · Traditional Surgical Instrument Service and Savings, Inc.09/14/2024SE
K240972Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC)NLH · Traditional Surgical Instrument Service and Savings, Inc.06/07/2024SE
K233825Reprocessed Webster Duo-Decapolar Diagnostic EP CatheterNLH · Traditional Innovative Health06/07/2024SE
K221067Medline ReNewal Reprocessed St. Jude Medical Livewire Steerable Electrophysiology CatheterNLH · Traditional Surgical Instrument Service and Savings, Inc.05/31/2023SE
K221854Reprocesses Umbilical CableNLH · Traditional Innovative Health, LLC08/06/2022SE
K211276Reprocessed Dynamic Tip and XT Steerable Diagnostic Electrophysiology CathetersNLH · Traditional Innovative Health, LLC09/15/2021SE

More from Innovative Health, LLC

510(k)DeviceDecision
K250314Medline ReNewal Reprocessed Abbott Agilis Nxt Steerable IntroducerPNE · Traditional 12/19/2025SE
K250772Medline ReNewal Reprocessed Boston Scientific Dynamic XT Unidirectional Steerable…NLH · Traditional 07/11/2025SE
K250545Medline ReNewal Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound…OWQ · Traditional 06/05/2025SE
K243101Medline ReNewal Reprocessed Siemens ACUSON AcuNav 10F Ultrasound Catheter (for Siemens…OWQ · Traditional 03/10/2025SE
K242225Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic CatheterNLH · Traditional 11/29/2024SE
K241156Medline ReNewal Reprocessed St. Jude Medical Response Electrophysiology Catheter…NLH · Traditional 09/14/2024SE
K234064Medline ReNewal Reprocessed Siemens ACUSON AcuNav 8F Ultrasound Catheter (for Siemens…OWQ · Traditional 09/10/2024SE
K240972Medline ReNewal Reprocessed Medtronic Achieve Catheter Connecting Cable (2ACHC)NLH · Traditional 06/07/2024SE
K232511Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)NUJ · Traditional 04/29/2024SE
K221067Medline ReNewal Reprocessed St. Jude Medical Livewire Steerable Electrophysiology CatheterNLH · Traditional 05/31/2023SE

Questions and answers

When was Medline ReNewal Reprocessed Boston Scientific Dynamic Tip Unidirectional Steerable Diagnostic Catheter cleared by the FDA?

Medline ReNewal Reprocessed Boston Scientific Dynamic Tip Unidirectional Steerable Diagnostic Catheter (K252405) received a 510(k) decision of Substantially Equivalent on November 26, 2025, 118 days after the submission was received.

What is the product code of K252405?

The FDA product code is NLH – Catheter, Recording, Electrode, Reprocessed, a Class II (moderate risk) device regulated under 21 CFR 870.1220.