510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K020854Substantially Equivalent

Modification to Fox Pta Catheter

Jomed AG, Rockville MD / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K020854 is the FDA 510(k) clearance record for MODIFICATION TO FOX PTA CATHETER, a class II device, cleared for Jomed AG on under FDA product code LIT (Catheter, Angioplasty, Peripheral, Transluminal). FDA records list 3 510(k) clearances for Jomed AG, from to . As of , FDA records show no recalls naming K020854.

Clearance record

Decision date
Received
(27 days to decision)
Product code
LIT Catheter, Angioplasty, Peripheral, Transluminal
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Jomed AG 1700 Rockville Pike,Suite# 400, Rockville MD
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LIT

Trailing 12 months
5 clearances under product code LIT in the twelve months to October 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code LIT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20262
October 20260