Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K832132Substantially Equivalent

Sera-Tek Mycoplasma Antibody Test

Miles Laboratories, Inc., Walker MI / Traditional, Substantially Equivalent

K832132 is the FDA 510(k) clearance record for SERA-TEK MYCOPLASMA ANTIBODY TEST, a class I device, cleared for Miles Laboratories, Inc. on under FDA product code GSB (Antigens, Cf, All, Mycoplasma Spp.). FDA records list 158 510(k) clearances for Miles Laboratories, Inc., from to . As of , FDA records show no recalls naming K832132.

Clearance record

Decision date
Received
(81 days to decision)
Product code
GSB Antigens, Cf, All, Mycoplasma Spp.
Regulation
21 CFR 866.3375
Device class
Class I
Review panel
Microbiology
Applicant
Miles Laboratories, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code GSB

Trailing 12 months

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

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