SAS SALMONELLA O FACTOR 6 ANTISERUM
K-Number: K961951 · 1996-06-18
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Device Summary
Frequently Asked Questions
What is the SAS SALMONELLA O FACTOR 6 ANTISERUM?
SAS SALMONELLA O FACTOR 6 ANTISERUM is a medical device that received FDA 510(k) clearance on 1996-06-18. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K961951.
When did SAS SALMONELLA O FACTOR 6 ANTISERUM receive FDA 510(k) clearance?
SAS SALMONELLA O FACTOR 6 ANTISERUM received FDA 510(k) clearance on 1996-06-18, under 510(k) number K961951.
Who is the listed applicant for SAS SALMONELLA O FACTOR 6 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 FACTOR 6 ANTISERUM?
The FDA product code for SAS SALMONELLA O FACTOR 6 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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