SAS BRUCELLA SUIS ANTISERUM— 510(k) K952144

Name: FDA 510(k) clearance K952144
Creator: U.S. Food and Drug Administration
Published: 1995-07-21

Substantially Equivalent

Sa Scientific, Inc.

FDA 510(k) clearance K952144 for SAS BRUCELLA SUIS ANTISERUM, Substantially Equivalent on 1995-07-21. Applicant: Sa Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Sa Scientific, Inc.
Product code: Code GSM
Device class: Class 2
Regulation: 21 CFR 866.3085
Advisory panel: Microbiology
Date received: 1995-05-08
Decision date: 1995-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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K952143 — SAS BRUCELLA MELITENSIS ANTISERUM1995-07-21
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Data sourced from openFDA. This site is unofficial and independent of the FDA.