Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SAS SALMONELLA H B ANTISERUM

K-Number: K951069 · 1995-06-09

Decision Date1995-06-09
Product CodeGRM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SAS SALMONELLA H B 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 1995-06-09 under 510(k) number K951069. 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 H B ANTISERUM?

SAS SALMONELLA H B ANTISERUM is a medical device that received FDA 510(k) clearance on 1995-06-09. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K951069.

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

SAS SALMONELLA H B ANTISERUM received FDA 510(k) clearance on 1995-06-09, under 510(k) number K951069.

Who is the listed applicant for SAS SALMONELLA H B 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 B ANTISERUM?

The FDA product code for SAS SALMONELLA H B 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

View on FDA Database →

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

↑