SAS FEBRILE ANTIGEN SET
K-Number: K952131 · 1995-07-17
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Device Summary
Frequently Asked Questions
What is the SAS FEBRILE ANTIGEN SET?
SAS FEBRILE ANTIGEN SET is a medical device that received FDA 510(k) clearance on 1995-07-17. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K952131.
When did SAS FEBRILE ANTIGEN SET receive FDA 510(k) clearance?
SAS FEBRILE ANTIGEN SET received FDA 510(k) clearance on 1995-07-17, under 510(k) number K952131.
Who is the listed applicant for SAS FEBRILE ANTIGEN SET?
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 FEBRILE ANTIGEN SET?
The FDA product code for SAS FEBRILE ANTIGEN SET is GSO.
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: GSO)
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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