SAS BRUCELLA MELITENSIS ANTISERUM
K-Number: K952143 · 1995-07-21
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Device Summary
Frequently Asked Questions
What is the SAS BRUCELLA MELITENSIS ANTISERUM?
SAS BRUCELLA MELITENSIS ANTISERUM is a medical device that received FDA 510(k) clearance on 1995-07-21. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K952143.
When did SAS BRUCELLA MELITENSIS ANTISERUM receive FDA 510(k) clearance?
SAS BRUCELLA MELITENSIS ANTISERUM received FDA 510(k) clearance on 1995-07-21, under 510(k) number K952143.
Who is the listed applicant for SAS BRUCELLA MELITENSIS 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 BRUCELLA MELITENSIS ANTISERUM?
The FDA product code for SAS BRUCELLA MELITENSIS ANTISERUM is GSM.
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: GSM)
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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