510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955722Substantially Equivalent

Flexon Temporary Cardiac Pacer Lead

Davis & Geck, Inc., Danbury CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955722 is the FDA 510(k) clearance record for FLEXON TEMPORARY CARDIAC PACER LEAD, a class II device, cleared for Davis & Geck, Inc. on under FDA product code LDF (Electrode, Pacemaker, Temporary). FDA records list 45 510(k) clearances for Davis & Geck, Inc., from to . As of , FDA records show no recalls naming K955722.

Clearance record

Decision date
Received
(88 days to decision)
Product code
LDF Electrode, Pacemaker, Temporary
Regulation
21 CFR 870.3680
Device class
Class II
Review panel
Cardiovascular
Applicant
Davis & Geck, Inc. One Casper St., Danbury CT
510(k) summary
Statement
Third party review
No

Clearances, product code LDF

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