510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K930235Substantially Equivalent

Hemochron/factor VI Whole Blood Factor VIII Assay

Technidyne Corp., Edison NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930235 is the FDA 510(k) clearance record for HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY, a class II device, cleared for Technidyne Corp. on under FDA product code GGP (Test, Qualitative And Quantitative Factor Deficiency). FDA records list 2 510(k) clearances for Technidyne Corp. As of , FDA records show no recalls naming K930235.

Clearance record

Decision date
Received
(240 days to decision)
Product code
GGP Test, Qualitative And Quantitative Factor Deficiency
Regulation
21 CFR 864.7290
Device class
Class II
Review panel
Hematology
Applicant
Technidyne Corp. 23 Nevsky St., Edison NJ
510(k) summary
Statement
Third party review
No

Clearances, product code GGP

Trailing 12 months

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

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