510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934080Substantially Equivalent

Urinary Drainage Bag

Kit Pak, Inc., Elk Grove Village IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934080 is the FDA 510(k) clearance record for URINARY DRAINAGE BAG, a class I device, cleared for Kit Pak, Inc. on under FDA product code EYT (Sheath, Corrugated Rubber, For Nonindwelling Catheter, Sterile). FDA records list 13 510(k) clearances for Kit Pak, Inc., from to . As of , FDA records show no recalls naming K934080.

Clearance record

Decision date
Received
(271 days to decision)
Product code
EYT Sheath, Corrugated Rubber, For Nonindwelling Catheter, Sterile
Regulation
21 CFR 876.5250
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Kit Pak, Inc. 825 Chase Ave., Elk Grove Village IL
510(k) summary
Statement
Third party review
No

Clearances, product code EYT

Trailing 12 months

FDA records hold no clearances under product code EYT in the trailing twelve months.

FDA records show no clearances under product code EYT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EYT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260