Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar Temporary Atrial Pacing Lead, Streamline 6494 Unipolar Temporary Myocardial Pacing Wire, Streamline 6495 Unipolar Temporary Myocardial Pacing Lead

FDA 510(k) K190716 · Medtronic

Substantially Equivalent

510(k) numberK190716

Submission

Device name
Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar Temporary Atrial Pacing Lead, Streamline 6494 Unipolar Temporary Myocardial Pacing Wire, Streamline 6495 Unipolar Temporary Myocardial Pacing Lead
Applicant
Medtronic
Santa Ana, CA, US
Received
March 19, 2019
Decision date
August 8, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LDF – Electrode, Pacemaker, Temporary
Device class
Class II (moderate risk)
Regulation
21 CFR 870.3680
Specialty
Cardiovascular
Life-sustaining
Yes

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K251186Bard® Temporary Pacing Electrode Catheter Needle / Cannula (Introducer)LDF · Special C.R. Bard, Inc.05/15/2025SE
K241334Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes…LDF · Traditional C.R. Bard, Inc.01/31/2025SE
K241199Rotatable Connector (5944RL)LDF · Traditional Shenzhen Launch Electrical Co., Ltd.01/23/2025SE
K242705Streamline Unipolar Pediatric Temporary Pacing Lead (6491) Streamline Unipolar Temporary…LDF · Special Medtronic, Inc.01/17/2025SE
K232261TME Temporary Myocardial ElectrodeLDF · Traditional Osypka AG04/26/2024SE
K173923Temporary Cardiac Pacing WireLDF · Traditional ETHICON, Inc.08/02/2018SE
K171253Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar…LDF · Special Medtronic05/25/2017SE
K161873Pacel Flow Directed Pacing CatheterLDF · Traditional St Jude Medical11/22/2016SE

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Questions and answers

When was Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar Temporary Atrial Pacing Lead, Streamline 6494 Unipolar Temporary Myocardial Pacing Wire, Streamline 6495 Unipolar Temporary Myocardial Pacing Lead cleared by the FDA?

Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar Temporary Atrial Pacing Lead, Streamline 6494 Unipolar Temporary Myocardial Pacing Wire, Streamline 6495 Unipolar Temporary Myocardial Pacing Lead (K190716) received a 510(k) decision of Substantially Equivalent on August 8, 2019, 142 days after the submission was received.

What is the product code of K190716?

The FDA product code is LDF – Electrode, Pacemaker, Temporary, a Class II (moderate risk) device regulated under 21 CFR 870.3680.