510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K902342Substantially Equivalent

Unipolar Pediatric Temporary Pacing Lead, #6491

Medtronic, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902342 is the FDA 510(k) clearance record for UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD, #6491, a class II device, cleared for Medtronic Vascular on under FDA product code LDF (Electrode, Pacemaker, Temporary). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K902342.

Clearance record

Decision date
Received
(144 days to decision)
Product code
LDF Electrode, Pacemaker, Temporary
Regulation
21 CFR 870.3680
Device class
Class II
Review panel
Cardiovascular
Applicant
Medtronic Vascular 800 53rd Ave., NE, Minneapolis MN
Third party review
No

Clearances, product code LDF

Trailing 12 months
1 clearance under product code LDF in the twelve months to November 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LDF, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260
November 20260