510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K000753Substantially Equivalent

Cordis 13F Catheter Sheath Introducer

Cordis US Corp., Miami Lakes FL / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K000753 is the FDA 510(k) clearance record for CORDIS 13F CATHETER SHEATH INTRODUCER, a class II device, cleared for Cordis Corp. on under FDA product code DRF (Catheter, Electrode Recording, Or Probe, Electrode Recording). FDA records list 332 510(k) clearances for Cordis US Corp., from to . As of , FDA records show no recalls naming K000753.

Clearance record

Decision date
Received
(29 days to decision)
Product code
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
Regulation
21 CFR 870.1220
Device class
Class II
Review panel
Cardiovascular
Applicant
Cordis Corp. 14201 NW 60th Ave., Miami Lakes FL
510(k) summary
Summary
Third party review
No

Clearances, product code DRF

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