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
K802840Substantially Equivalent

Alpha-Antiplasm Assay

American Dade, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802840 is the FDA 510(k) clearance record for ALPHA-ANTIPLASM ASSAY, a class II device, cleared for American Dade on under FDA product code LGP (Assay, Alpha-2-Antiplasmin). FDA records list 149 510(k) clearances for American Dade, from to . As of , FDA records show no recalls naming K802840.

Clearance record

Decision date
Received
(97 days to decision)
Product code
LGP Assay, Alpha-2-Antiplasmin
Regulation
21 CFR 864.5425
Device class
Class II
Review panel
Hematology
Applicant
American Dade 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LGP

Trailing 12 months

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

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