510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K844280Substantially Equivalent

Travenol Value-Line Urinary Drainage Bag W/sterile

Travenol Laboratories, S.A., Deerfield IL / Traditional, Substantially Equivalent

K844280 is the FDA 510(k) clearance record for TRAVENOL VALUE-LINE URINARY DRAINAGE BAG W/STERILE, a class II device, cleared for Travenol Laboratories, S.A. on under FDA product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter). FDA records list 206 510(k) clearances for Travenol Laboratories, S.A., from to . As of , FDA records show no recalls naming K844280.

Clearance record

Decision date
Received
(42 days to decision)
Product code
KNX Collector, Urine, (And Accessories) For Indwelling Catheter
Regulation
21 CFR 876.5250
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Travenol Laboratories, S.A.
Third party review
No

Clearances, product code KNX

Trailing 12 months

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

FDA records show no clearances under product code KNX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KNX, 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