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

CRYOCHECK CLOT C

K Number: K040987 · Decision Jun 18, 2004
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
7
Review Days
64

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Basic Information

Device Name
CRYOCHECK CLOT C
K Number
K040987
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Precision Biologic, Inc.
Date Received
April 15, 2004
Decision Date
June 18, 2004
Product Code
GGP
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
GGP Test, Qualitative And Quantitative Factor Deficiency

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GGP), ordered by most recent decision date.

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Other Clearances by Precision Biologic, Inc.

K Number Device Name
K251440 CRYOcheck Chromogenic Factor VIII
K222831 CRYOcheck Factor VIII Deficient Plasma with VWF
K214002 CRYOcheck Chromogenic Factor IX
K183440 CRYOcheck FVIII Inhibitor Kit
K060284 CRYOCHECK CLOT APCR
K043571 CRYOCHECK CLOT S