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FDA 510(k)

SAS SALMONELLA H E COMPLEX ANTISERUM

K-Number: K955215 · 1996-02-07

ApplicantSa Scientific, Inc.
Decision Date1996-02-07
Product CodeGNC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SAS SALMONELLA H E COMPLEX 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 1996-02-07 under 510(k) number K955215. The device is classified under product code GNC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAS SALMONELLA H E COMPLEX ANTISERUM?

SAS SALMONELLA H E COMPLEX ANTISERUM is a medical device that received FDA 510(k) clearance on 1996-02-07. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K955215.

When did SAS SALMONELLA H E COMPLEX ANTISERUM receive FDA 510(k) clearance?

SAS SALMONELLA H E COMPLEX ANTISERUM received FDA 510(k) clearance on 1996-02-07, under 510(k) number K955215.

Who is the listed applicant for SAS SALMONELLA H E COMPLEX 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 H E COMPLEX ANTISERUM?

The FDA product code for SAS SALMONELLA H E COMPLEX ANTISERUM is GNC.

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.

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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.

K100227SAS FLUALERT A&B, SAS INFLUENZA A TESTK080380SAS INFLUENZA A & B TESTK041439SAS INFLUENZA B TESTK041441SAS INFLUENZA A TESTK030628SAS RSV CONTROL KITK022845SAS RSV TEST

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Related Devices (Code: GNC)

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.

K972388VISTA ANTIGEN SALMONELLA O GROUP CLee Laboratories, Inc.K972395VISTA ANTIGEN SALMONELLA O GROUP DLee Laboratories, Inc.K972389VISTA ANTIGEN SALMONELLA H DLee Laboratories, Inc.K972387VISTA ANTIGEN SALMONELLA O GROUP ALee Laboratories, Inc.K972386VISTA ANTIGEN SALMONELLA O GROUP BLee Laboratories, Inc.K972391VISTA ANTIGEN SALMONELLA H BLee Laboratories, Inc.

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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