FDA 510(k) Substantially Equivalent 🇺🇸 United States

COMPLUS VARIOUS FORMS

K Number: K831039 · Decision May 27, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
30
Review Days
57

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Basic Information

Device Name
COMPLUS VARIOUS FORMS
K Number
K831039
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Parker Laboratories, Inc.
Date Received
March 31, 1983
Decision Date
May 27, 1983
Advisory Committee
Unknown
Review Advisory Committee
DE
Third Party
N

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