510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872360Substantially Equivalent

Data-Fi Fibrin(ogen) Degradation Prod.(fdp)det Set

American Dade, Santa Ana CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872360 is the FDA 510(k) clearance record for DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET, a class II device, cleared for American Dade on under FDA product code GHH (Fibrin Split Products). FDA records list 149 510(k) clearances for American Dade, from to . As of , FDA records show one recall naming K872360.

Clearance record

Decision date
Received
(18 days to decision)
Product code
GHH Fibrin Split Products
Regulation
21 CFR 864.7320
Device class
Class II
Review panel
Hematology
Applicant
American Dade P.O. Box 25101, Santa Ana CA
Third party review
No

Clearances, product code GHH

Trailing 12 months

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

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