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FDA 510(k)

SAS SHIGELLA BOYDII GROUP C2 ANTISERUM

K-Number: K953329 · 1995-08-02

Decision Date1995-08-02
Product CodeGNB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SAS SHIGELLA BOYDII GROUP C2 ANTISERUM is the device name listed in this FDA 510(k) record. The listed applicant is Sa Scientific, Inc.. It received FDA 510(k) clearance on 1995-08-02 under 510(k) number K953329. The device is classified under product code GNB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAS SHIGELLA BOYDII GROUP C2 ANTISERUM?

SAS SHIGELLA BOYDII GROUP C2 ANTISERUM is a medical device that received FDA 510(k) clearance on 1995-08-02. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K953329.

When did SAS SHIGELLA BOYDII GROUP C2 ANTISERUM receive FDA 510(k) clearance?

SAS SHIGELLA BOYDII GROUP C2 ANTISERUM received FDA 510(k) clearance on 1995-08-02, under 510(k) number K953329.

Who is the listed applicant for SAS SHIGELLA BOYDII GROUP C2 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 SHIGELLA BOYDII GROUP C2 ANTISERUM?

The FDA product code for SAS SHIGELLA BOYDII GROUP C2 ANTISERUM is GNB.

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.

View all 199 devices →

Related Devices (Code: GNB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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