510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K893608Substantially Equivalent

Actichrome Atiii Kit

American Diagnostic Corp., New York NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893608 is the FDA 510(k) clearance record for ACTICHROME ATIII KIT, a class II device, cleared for American Diagnostic Corp. on under FDA product code JBQ (Antithrombin Iii Quantitation). FDA records list 39 510(k) clearances for American Diagnostic Corp., from to . As of , FDA records show no recalls naming K893608.

Clearance record

Decision date
Received
(44 days to decision)
Product code
JBQ Antithrombin Iii Quantitation
Regulation
21 CFR 864.7060
Device class
Class II
Review panel
Hematology
Applicant
American Diagnostic Corp. 49 E. 68th St., New York NY
Third party review
No

Clearances, product code JBQ

Trailing 12 months

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

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