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
K913330Substantially Equivalent

Urine Collection Kit/device

Medical Implements, Inc., Richmond VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913330 is the FDA 510(k) clearance record for URINE COLLECTION KIT/DEVICE, a class I device, cleared for Medical Implements, Inc. on under FDA product code KHP (Acid, Lactic, Enzymatic Method). FDA records list 2 510(k) clearances for Medical Implements, Inc., from to . As of , FDA records show no recalls naming K913330.

Clearance record

Decision date
Received
(32 days to decision)
Product code
KHP Acid, Lactic, Enzymatic Method
Regulation
21 CFR 862.1450
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Medical Implements, Inc. 11341 Business Center Dr., Richmond VA
510(k) summary
Statement
Third party review
No

Clearances, product code KHP

Trailing 12 months

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

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