510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952622Substantially Equivalent

Cryo Check Normal Human Reference Plasma

Precision Biologicals, Inc., Dartmouth, Nova Scotia, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952622 is the FDA 510(k) clearance record for CRYO CHECK NORMAL HUMAN REFERENCE PLASMA, a class II device, cleared for Precision Biologicals, Inc. on under FDA product code GGN (Plasma, Coagulation Control). FDA records list 20 510(k) clearances for Precision Biologicals, Inc., from to . As of , FDA records show no recalls naming K952622.

Clearance record

Decision date
Received
(144 days to decision)
Product code
GGN Plasma, Coagulation Control
Regulation
21 CFR 864.5425
Device class
Class II
Review panel
Hematology
Applicant
Precision Biologicals, Inc. 900 Windmill Rd., Dartmouth, Nova Scotia, CA
510(k) summary
Statement
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