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
K772151Substantially Equivalent

Urinary Vma - Screen Test Kit

Eppendorf-Brinkmann, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K772151 is the FDA 510(k) clearance record for URINARY VMA - SCREEN TEST KIT, a class I device, cleared for Eppendorf-Brinkmann, Inc. on under FDA product code CDF (Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin). FDA records list 4 510(k) clearances for Eppendorf-Brinkmann, Inc., from to . As of , FDA records show no recalls naming K772151.

Clearance record

Decision date
Received
(15 days to decision)
Product code
CDF Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin
Regulation
21 CFR 862.1795
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Eppendorf-Brinkmann, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CDF

Trailing 12 months

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

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