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FDA 510(k)

GISH TUBING AND CONNECTORS WITH GBS COATING

K-Number: K030077 · 2003-03-14

Decision Date2003-03-14
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GISH TUBING AND CONNECTORS WITH GBS COATING 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 2003-03-14 under 510(k) number K030077. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GISH TUBING AND CONNECTORS WITH GBS COATING?

GISH TUBING AND CONNECTORS WITH GBS COATING is a medical device that received FDA 510(k) clearance on 2003-03-14. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K030077.

When did GISH TUBING AND CONNECTORS WITH GBS COATING receive FDA 510(k) clearance?

GISH TUBING AND CONNECTORS WITH GBS COATING received FDA 510(k) clearance on 2003-03-14, under 510(k) number K030077.

Who is the listed applicant for GISH TUBING AND CONNECTORS WITH GBS COATING?

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 TUBING AND CONNECTORS WITH GBS COATING?

The FDA product code for GISH TUBING AND CONNECTORS WITH GBS COATING is DTL.

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: DTL)

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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