Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K945857Substantially Equivalent

Protein C Deficient Plasma

George King Bio-Medical, Inc., Overland Park KS / Traditional, Substantially Equivalent

K945857 is the FDA 510(k) clearance record for PROTEIN C DEFICIENT PLASMA, a class II device, cleared for George King Bio-Medical, Inc. on under FDA product code GJT (Plasma, Coagulation Factor Deficient). FDA records list 5 510(k) clearances for George King Bio-Medical, Inc., from to . As of , FDA records show no recalls naming K945857.

Clearance record

Decision date
Received
(340 days to decision)
Product code
GJT Plasma, Coagulation Factor Deficient
Regulation
21 CFR 864.7290
Device class
Class II
Review panel
Hematology
Applicant
George King Bio-Medical, Inc. 11771 W. 112th St., Overland Park KS
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