FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

CRYO CHECK ABNORMAL REFERENCE CHECK I & II

K Number: K952624 · Decision Oct 30, 1995
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
39
Applicant Total
20
Review Days
144

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Basic Information

Device Name
CRYO CHECK ABNORMAL REFERENCE CHECK I & II
K Number
K952624
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5425
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Precision Biologicals, Inc.
Date Received
June 8, 1995
Decision Date
October 30, 1995
Product Code
GGC
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GGC Control, Plasma, Abnormal

Similar 510(k) Clearances

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Other Clearances by Precision Biologicals, Inc.

K Number Device Name
K981173 CRYO CHECK FACTOR XI DEFICIENT PLASMA, MODEL FDP11-10 (1.OML) AND FDP11-15 (1.5ML)
K982062 CRYO-CHECK PNP PLATELET LYSATE, MODEL PNP-10
K981174 CRYO CHECK FACTOR XII DEFICIENT PLASMA MODEL FDP12-10 (1.0ML) AND FDP12-15 (1.5ML)
K971219 CRYO CHECK INR VALIDATION SET
K971222 CRYO CHECK APC RESISTANT PLASMA
K971223 CRYO CHECK FACTOR V DEFICIENT PLASMA
K971227 CRYO CHECK FACTOR X DEFICIENT PLASMA
K971226 CRYO CHECK FACTOR IX DEFICIENT PLASMA
K971225 CRYO CHECK FACTOR VIII DEFICIENT PLASMA
K971224 CRYO CHECK FACTOR VII DEFICIENT PLASMA
Search all 20 clearances from Precision Biologicals, Inc. →