Unipolar Temporary Myocardial Pacing Wire, 6493

FDA 510(k) K922269 · The Heart Valve Div. Medtronic Cardiovascular Surg

Substantially Equivalent

510(k) numberK922269

Submission

Device name
Unipolar Temporary Myocardial Pacing Wire, 6493
Applicant
The Heart Valve Div. Medtronic Cardiovascular Surg
Minneapolis, MN, US
Received
May 14, 1992
Decision date
November 23, 1992
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
K190716Streamline 6491 Unipolar Pediatric Temporary Pacing Lead, Streamline 6492 Unipolar…LDF · Traditional Medtronic08/08/2019SE
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

More from Medtronic

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K960356Posterior Annuloplasty Band (Model 607)KRH · Traditional 08/27/1996ST
K944956Unipolar Pediatric Temporary Pacing Lead, Model 6491LDF · Traditional 07/14/1995SE
K914602Duran Flex Annuloplasty Ring/Obtur H601H, ModifiedKRH · Traditional 11/22/1991SE

Questions and answers

When was Unipolar Temporary Myocardial Pacing Wire, 6493 cleared by the FDA?

Unipolar Temporary Myocardial Pacing Wire, 6493 (K922269) received a 510(k) decision of Substantially Equivalent on November 23, 1992, 193 days after the submission was received.

What is the product code of K922269?

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