510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K120977Substantially Equivalent

Directcheck Control for Hemochron Jr. Microcoagulation Systems Act-Lr Cuvette Directcheck Controls for Hemochron Jr. Mic

Accriva Diagnostics, Inc., Edison NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K120977 is the FDA 510(k) clearance record for DIRECTCHECK CONTROL FOR HEMOCHRON JR. MICROCOAGULATION SYSTEMS ACT-LR CUVETTE DIRECTCHECK CONTROLS FOR HEMOCHRON JR. MIC, a class II device, cleared for International Technidyne Corp. on under FDA product code GGN (Plasma, Coagulation Control). FDA records list 51 510(k) clearances for Accriva Diagnostics, Inc., from to . As of , FDA records show no recalls naming K120977.

Clearance record

Decision date
Received
(457 days to decision)
Product code
GGN Plasma, Coagulation Control
Regulation
21 CFR 864.5425
Device class
Class II
Review panel
Hematology
Applicant
International Technidyne Corp. 23 Nevsky St., Edison NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GGN

Trailing 12 months

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

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