SAS SALMONELLA O FACTOR 22 ANTISERUM &/OR SAS SALMONELLA O GROUP G1 FACTOR 22 ANTISERUM— 510(k) K960127

Name: FDA 510(k) clearance K960127
Creator: U.S. Food and Drug Administration
Published: 1996-03-06

Substantially Equivalent

Sa Scientific, Inc.

FDA 510(k) clearance K960127 for SAS SALMONELLA O FACTOR 22 ANTISERUM &/OR SAS SALMONELLA O GROUP G1 FACTOR 22 ANTISERUM, Substantially Equivalent on 1996-03-06. Applicant: Sa Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Sa Scientific, Inc.
Product code: Code GRM
Device class: Class 2
Regulation: 21 CFR 866.3550
Advisory panel: Microbiology
Date received: 1996-01-11
Decision date: 1996-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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K961951 — SAS SALMONELLA O FACTOR 6 ANTISERUM1996-06-18
K961952 — SAS SALMONELLA O FACTOR /O GROUP A FACTOR 2 ANTISERUMS1996-06-18

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