510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K772133Substantially Equivalent

Urine Specimen Collecting Device

Kendall Research Center, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K772133 is the FDA 510(k) clearance record for URINE SPECIMEN COLLECTING DEVICE, a class II device, cleared for Kendall Research Center on under FDA product code FCN (Urinary Drainage Collection Kit, For Indwelling Catheter). FDA records list 14 510(k) clearances for Kendall Research Center, from to . As of , FDA records show no recalls naming K772133.

Clearance record

Decision date
Received
(14 days to decision)
Product code
FCN Urinary Drainage Collection Kit, For Indwelling Catheter
Regulation
21 CFR 876.5250
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Kendall Research Center 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FCN

Trailing 12 months

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

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