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
K800926Substantially Equivalent

Thromboquik Thrombin Reagent Prod. #3551

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

K800926 is the FDA 510(k) clearance record for THROMBOQUIK THROMBIN REAGENT PROD. #3551, a class II device, cleared for General Diagnostics on under FDA product code GJA (Test, Thrombin Time). FDA records list 39 510(k) clearances for General Diagnostics, from to . As of , FDA records show no recalls naming K800926.

Clearance record

Decision date
Received
(17 days to decision)
Product code
GJA Test, Thrombin Time
Regulation
21 CFR 864.7875
Device class
Class II
Review panel
Hematology
Applicant
General Diagnostics 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GJA

Trailing 12 months

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

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