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FDA 510(k)

CENTRAL VENOUS ACCESS CATHETER CVAC-XX

K-Number: K841587 · 1984-06-13

ApplicantGish Biomedical, Inc.
Decision Date1984-06-13
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL VENOUS ACCESS CATHETER CVAC-XX 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 1984-06-13 under 510(k) number K841587. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRAL VENOUS ACCESS CATHETER CVAC-XX?

CENTRAL VENOUS ACCESS CATHETER CVAC-XX is a medical device that received FDA 510(k) clearance on 1984-06-13. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K841587.

When did CENTRAL VENOUS ACCESS CATHETER CVAC-XX receive FDA 510(k) clearance?

CENTRAL VENOUS ACCESS CATHETER CVAC-XX received FDA 510(k) clearance on 1984-06-13, under 510(k) number K841587.

Who is the listed applicant for CENTRAL VENOUS ACCESS CATHETER CVAC-XX?

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 CENTRAL VENOUS ACCESS CATHETER CVAC-XX?

The FDA product code for CENTRAL VENOUS ACCESS CATHETER CVAC-XX is DQY.

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Other records listing Gish Biomedical, Inc. as applicant

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Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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.

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