510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K040362Substantially Equivalent

Diapharma Factor X Kit

Diapharma Group, Inc., West Chester OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K040362 is the FDA 510(k) clearance record for DIAPHARMA FACTOR X KIT, a class II device, cleared for Diapharma Group, Inc. on under FDA product code GJT (Plasma, Coagulation Factor Deficient). FDA records list one 510(k) clearance for Diapharma Group, Inc. As of , FDA records show no recalls naming K040362.

Clearance record

Decision date
Received
(150 days to decision)
Product code
GJT Plasma, Coagulation Factor Deficient
Regulation
21 CFR 864.7290
Device class
Class II
Review panel
Hematology
Applicant
Diapharma Group, Inc. 8948 Beckett Rd., West Chester OH
510(k) summary
Statement
Third party review
No

Clearances, product code GJT

Trailing 12 months

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

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