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

SAS SALMONELLA O FACTOR 46 ANTISERUM

K Number: K960460 · Decision Mar 6, 1996
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
68
Applicant Total
199
Review Days
36

Basic Information

Device Name
SAS SALMONELLA O FACTOR 46 ANTISERUM
K Number
K960460
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3550
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SA SCIENTIFIC, INC.
Date Received
January 30, 1996
Decision Date
March 6, 1996
Product Code
GRM
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
GRM Antisera, All Groups, Salmonella Spp.

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