510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K032613Substantially Equivalent

Temporary Transvenous Pacemaker Placement Assist Device

Peter M. Rothenberg, M.D., San Clemente CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K032613 is the FDA 510(k) clearance record for TEMPORARY TRANSVENOUS PACEMAKER PLACEMENT ASSIST DEVICE, a class II device, cleared for Peter M. Rothenberg, M.D. on under FDA product code LDF (Electrode, Pacemaker, Temporary). FDA records list one 510(k) clearance for Peter M. Rothenberg, M.D. As of , FDA records show no recalls naming K032613.

Clearance record

Decision date
Received
(87 days to decision)
Product code
LDF Electrode, Pacemaker, Temporary
Regulation
21 CFR 870.3680
Device class
Class II
Review panel
Cardiovascular
Applicant
Peter M. Rothenberg, M.D. 657 Camino De Los Mares, San Clemente CA
510(k) summary
Summary PDF
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