Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K813359Substantially Equivalent

Myco-Immune Tm Histoplasmin Latex Aggl

American Scientific Products, Mchenry IL / Traditional, Substantially Equivalent

K813359 is the FDA 510(k) clearance record for MYCO-IMMUNE TM HISTOPLASMIN LATEX AGGL, a class II device, cleared for American Scientific Products on under FDA product code GMJ (Antigens, Histoplasma Capsulatum, All). FDA records list 28 510(k) clearances for American Scientific Products, from to . As of , FDA records show no recalls naming K813359.

Clearance record

Decision date
Received
(31 days to decision)
Product code
GMJ Antigens, Histoplasma Capsulatum, All
Regulation
21 CFR 866.3320
Device class
Class II
Review panel
Microbiology
Applicant
American Scientific Products 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GMJ

Trailing 12 months

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

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