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FDA 510(k)

GISH ARTERIAL FILTER

K-Number: K914791 · 1993-04-06

Decision Date1993-04-06
Product CodeDTM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GISH ARTERIAL FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Gish Biomedical, Inc.. It received FDA 510(k) clearance on 1993-04-06 under 510(k) number K914791. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GISH ARTERIAL FILTER?

GISH ARTERIAL FILTER is a medical device that received FDA 510(k) clearance on 1993-04-06. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K914791.

When did GISH ARTERIAL FILTER receive FDA 510(k) clearance?

GISH ARTERIAL FILTER received FDA 510(k) clearance on 1993-04-06, under 510(k) number K914791.

Who is the listed applicant for GISH ARTERIAL FILTER?

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

What is the FDA product code for GISH ARTERIAL FILTER?

The FDA product code for GISH ARTERIAL FILTER is DTM.

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 Gish Biomedical, 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 75 devices →

Related Devices (Code: DTM)

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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