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)

STREP A NEGATIVE CONTROL

K-Number: K924461 · 1993-12-02

Decision Date1993-12-02
Product CodeGTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

STREP A NEGATIVE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Biotech, Inc.. It received FDA 510(k) clearance on 1993-12-02 under 510(k) number K924461. The device is classified under product code GTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STREP A NEGATIVE CONTROL?

STREP A NEGATIVE CONTROL is a medical device that received FDA 510(k) clearance on 1993-12-02. The listed applicant is Pacific Biotech, Inc.. The 510(k) number is K924461.

When did STREP A NEGATIVE CONTROL receive FDA 510(k) clearance?

STREP A NEGATIVE CONTROL received FDA 510(k) clearance on 1993-12-02, under 510(k) number K924461.

Who is the listed applicant for STREP A NEGATIVE CONTROL?

The FDA 510(k) record lists Pacific Biotech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STREP A NEGATIVE CONTROL?

The FDA product code for STREP A NEGATIVE CONTROL is GTZ.

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 Pacific Biotech, 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 29 devices →

Related Devices (Code: GTZ)

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.

↑