Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K770092Substantially Equivalent

Herpesivirus Test (Type L & 2)

Microbiological Research Corp., Mchenry IL / Traditional, Substantially Equivalent

K770092 is the FDA 510(k) clearance record for HERPESIVIRUS TEST (TYPE L & 2), a class II device, cleared for Microbiological Research Corp. on under FDA product code GOL (Antigen, Ha (Including Ha Control), Rubella). FDA records list 14 510(k) clearances for Microbiological Research Corp., from to . As of , FDA records show no recalls naming K770092.

Clearance record

Decision date
Received
(43 days to decision)
Product code
GOL Antigen, Ha (Including Ha Control), Rubella
Regulation
21 CFR 866.3510
Device class
Class II
Review panel
Microbiology
Applicant
Microbiological Research Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GOL

Trailing 12 months

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

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