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FDA 510(k)

EZTEST-GAS

K-Number: K930683 · 1997-03-04

Decision Date1997-03-04
Product CodeFRC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EZTEST-GAS is the device name listed in this FDA 510(k) record. The listed applicant is Sgm Biomedical, Inc.. It received FDA 510(k) clearance on 1997-03-04 under 510(k) number K930683. The device is classified under product code FRC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZTEST-GAS?

EZTEST-GAS is a medical device that received FDA 510(k) clearance on 1997-03-04. The listed applicant is Sgm Biomedical, Inc.. The 510(k) number is K930683.

When did EZTEST-GAS receive FDA 510(k) clearance?

EZTEST-GAS received FDA 510(k) clearance on 1997-03-04, under 510(k) number K930683.

Who is the listed applicant for EZTEST-GAS?

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

What is the FDA product code for EZTEST-GAS?

The FDA product code for EZTEST-GAS is FRC.

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.

Related Devices (Code: FRC)

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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