FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LANCER COAGENT HUMAN VACTOR VIII PLASMA

K Number: K812975 · Decision Nov 16, 1981
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
191
Review Days
24

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Basic Information

Device Name
LANCER COAGENT HUMAN VACTOR VIII PLASMA
K Number
K812975
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7290
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Sherwood Medical Co.
Date Received
October 23, 1981
Decision Date
November 16, 1981
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

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