510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K842660Substantially Equivalent

Anti-Schistosoma Species Kit

Amico Lab, Inc., TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842660 is the FDA 510(k) clearance record for ANTI-SCHISTOSOMA SPECIES KIT, a class I device, cleared for Amico Lab, Inc. on under FDA product code GNH (Antigen, Fluorescent Antibody Test, Schistosoma Mansoni). FDA records list 32 510(k) clearances for Amico Lab, Inc., from to . As of , FDA records show no recalls naming K842660.

Clearance record

Decision date
Received
(112 days to decision)
Product code
GNH Antigen, Fluorescent Antibody Test, Schistosoma Mansoni
Regulation
21 CFR 866.3600
Device class
Class I
Review panel
Microbiology
Applicant
Amico Lab, Inc.
Third party review
No

Clearances, product code GNH

Trailing 12 months

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

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