ViewFlex™ Eco Reprocessed ICE Catheter

FDA 510(k) K230934 · Abbott Medical

Substantially Equivalent

510(k) numberK230934

Submission

Device name
ViewFlex™ Eco Reprocessed ICE Catheter
Applicant
Abbott Medical
Minnetonka, MN, US
Received
April 3, 2023
Decision date
May 3, 2023
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OWQ – Reprocessed Intravascular Ultrasound Catheter
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1200
Specialty
Cardiovascular

For intracardiac and intraluminal visualization of cardiovascular anatomy and physiology.

Other 510(k)s with product code OWQ

510(k)DeviceApplicantDecision
K254149Reprocessed AcuNav CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on Siemens System…OWQ · Traditional Sterilmed, Inc.06/29/2026SE
K250545Medline ReNewal Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound…OWQ · Traditional Surgical Instrument Service and Savings, Inc.06/05/2025SE
K250592NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)OWQ · Traditional Northeast Scientific, Inc.05/12/2025SE
K243101Medline ReNewal Reprocessed Siemens ACUSON AcuNav 10F Ultrasound Catheter (for Siemens…OWQ · Traditional Surgical Instrument Service and Savings, Inc.03/10/2025SE
K234064Medline ReNewal Reprocessed Siemens ACUSON AcuNav 8F Ultrasound Catheter (for Siemens…OWQ · Traditional Surgical Instrument Service and Savings, Inc.09/10/2024SE
K232130Medline ReNewal Reprocessed ViewFlex Xtra ICE CatheterOWQ · Traditional Surgical Instrument Services and Savings, Inc.12/15/2023SE
K232584Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle…OWQ · Traditional Vein 360, LLC10/24/2023SE
K230928Vein360 Reprocessed Visions PV.018 Digital IVUS CatheterOWQ · Traditional Vein 360, LLC08/25/2023SE
K231621Reprocessed ViewFlex Xtra ICE Catheter (D087031)OWQ · Special Stryker Sustainability Solutions07/25/2023SE
K231588ViewFlex™ Eco Reprocessed ICE CatheterOWQ · Special Abbott Medical06/30/2023SE

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Questions and answers

When was ViewFlex™ Eco Reprocessed ICE Catheter cleared by the FDA?

ViewFlex™ Eco Reprocessed ICE Catheter (K230934) received a 510(k) decision of Substantially Equivalent on May 3, 2023, 30 days after the submission was received.

What is the product code of K230934?

The FDA product code is OWQ – Reprocessed Intravascular Ultrasound Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.1200.