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
K964757Substantially Equivalent

Contidrain Catheter

Contimed, Inc., Houlton WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K964757 is the FDA 510(k) clearance record for CONTIDRAIN CATHETER, a class II device, cleared for Contimed, Inc. on under FDA product code EZL (Catheter, Retention Type, Balloon). FDA records list one 510(k) clearance for Contimed, Inc. As of , FDA records show no recalls naming K964757.

Clearance record

Decision date
Received
(210 days to decision)
Product code
EZL Catheter, Retention Type, Balloon
Regulation
21 CFR 876.5130
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Contimed, Inc. 415 Valley View Trl., Houlton WI
510(k) summary
Summary
Third party review
No

Clearances, product code EZL

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