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FDA 510(k)

SAS SALMONELLA O GROUP H FACTORS 14,24,25 ANTISERUM

K-Number: K961964 · 1996-06-18

Decision Date1996-06-18
Product CodeGRM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SAS SALMONELLA O GROUP H FACTORS 14,24,25 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 1996-06-18 under 510(k) number K961964. The device is classified under product code GRM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAS SALMONELLA O GROUP H FACTORS 14,24,25 ANTISERUM?

SAS SALMONELLA O GROUP H FACTORS 14,24,25 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 K961964.

When did SAS SALMONELLA O GROUP H FACTORS 14,24,25 ANTISERUM receive FDA 510(k) clearance?

SAS SALMONELLA O GROUP H FACTORS 14,24,25 ANTISERUM received FDA 510(k) clearance on 1996-06-18, under 510(k) number K961964.

Who is the listed applicant for SAS SALMONELLA O GROUP H FACTORS 14,24,25 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 GROUP H FACTORS 14,24,25 ANTISERUM?

The FDA product code for SAS SALMONELLA O GROUP H FACTORS 14,24,25 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.

View all 199 devices →

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

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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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