SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM
K-Number: K960462 · 1996-03-06
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Device Summary
Frequently Asked Questions
What is the SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM?
SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM is a medical device that received FDA 510(k) clearance on 1996-03-06. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K960462.
When did SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM receive FDA 510(k) clearance?
SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM received FDA 510(k) clearance on 1996-03-06, under 510(k) number K960462.
Who is the listed applicant for SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM?
The FDA 510(k) record lists Sa Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM?
The FDA product code for SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM is GRM.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Sa Scientific, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GRM)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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