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

SAS SHIGELLA DYSENTERIAE GROUP A (1-7) ANTISERUM

K Number: K953316 · Decision Aug 4, 1995
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
40
Applicant Total
199
Review Days
22

Basic Information

Device Name
SAS SHIGELLA DYSENTERIAE GROUP A (1-7) ANTISERUM
K Number
K953316
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SA SCIENTIFIC, INC.
Date Received
July 13, 1995
Decision Date
August 4, 1995
Product Code
GNB
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
GNB Antisera, All Types, Shigella Spp.

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