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FDA 510(k)

TRIPLE LUMEN INFUSION CATHETER/ACCESS

K-Number: K841535 · 1984-05-23

ApplicantGish Biomedical, Inc.
Decision Date1984-05-23
Product Code
DecisionSubstantially Equivalent

Device Summary

TRIPLE LUMEN INFUSION CATHETER/ACCESS 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 1984-05-23 under 510(k) number K841535. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIPLE LUMEN INFUSION CATHETER/ACCESS?

TRIPLE LUMEN INFUSION CATHETER/ACCESS is a medical device that received FDA 510(k) clearance on 1984-05-23. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K841535.

When did TRIPLE LUMEN INFUSION CATHETER/ACCESS receive FDA 510(k) clearance?

TRIPLE LUMEN INFUSION CATHETER/ACCESS received FDA 510(k) clearance on 1984-05-23, under 510(k) number K841535.

Who is the listed applicant for TRIPLE LUMEN INFUSION CATHETER/ACCESS?

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

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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.

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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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