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

TEST, (IVDP) SMOOTHMUSCLE ANTIBODY

K Number: K760156 · Decision Jul 20, 1976
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
5
Applicant Total
135
Review Days
18

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Basic Information

Device Name
TEST, (IVDP) SMOOTHMUSCLE ANTIBODY
K Number
K760156
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5120
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Zeus Scientific, Inc.
Date Received
July 2, 1976
Decision Date
July 20, 1976
Product Code
DBE
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
DBE Antismooth Muscle Antibody, Indirect Immunofluorescent, Antigen, Control

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