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
K896052Substantially Equivalent

Fibrinogen Assay Kit

Medical Diagnostic Technologies, Inc., Ventura CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896052 is the FDA 510(k) clearance record for FIBRINOGEN ASSAY KIT, a class II device, cleared for Medical Diagnostic Technologies, Inc. on under FDA product code KQJ (System, Fibrinogen Determination). FDA records list 57 510(k) clearances for Medical Diagnostic Technologies, Inc., from to . As of , FDA records show no recalls naming K896052.

Clearance record

Decision date
Received
(22 days to decision)
Product code
KQJ System, Fibrinogen Determination
Regulation
21 CFR 864.7340
Device class
Class II
Review panel
Hematology
Applicant
Medical Diagnostic Technologies, Inc. 6020 Nicolle St., Suite D, Ventura CA
Third party review
No

Clearances, product code KQJ

Trailing 12 months

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

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