Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K881502Substantially Equivalent

Brewer Gel for Campylobacter

Fairleigh Dickinson Laboratories, Inc., Abilene TX / Traditional, Substantially Equivalent

K881502 is the FDA 510(k) clearance record for BREWER GEL FOR CAMPYLOBACTER, a class I device, cleared for Fairleigh Dickinson Laboratories, Inc. on under FDA product code KZJ (Device, Gas Generating). FDA records list 7 510(k) clearances for Fairleigh Dickinson Laboratories, Inc., from to . As of , FDA records show no recalls naming K881502.

Clearance record

Decision date
Received
(16 days to decision)
Product code
KZJ Device, Gas Generating
Regulation
21 CFR 866.2580
Device class
Class I
Review panel
Microbiology
Applicant
Fairleigh Dickinson Laboratories, Inc. 1249 Ambler Ave., Abilene TX
Third party review
No

Clearances, product code KZJ

Trailing 12 months

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

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