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FDA 510(k)

VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER

K-Number: K854610 · 1986-05-08

ApplicantGish Biomedical, Inc.
Decision Date1986-05-08
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER 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 1986-05-08 under 510(k) number K854610. 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 VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER?

VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER is a medical device that received FDA 510(k) clearance on 1986-05-08. The listed applicant is Gish Biomedical, Inc.. The 510(k) number is K854610.

When did VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER receive FDA 510(k) clearance?

VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER received FDA 510(k) clearance on 1986-05-08, under 510(k) number K854610.

Who is the listed applicant for VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER?

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 VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER?

The FDA product code for VASCULAR ACCESS PORT/CATH CAT.#VP-XXXX VASPORT SER is DQY.

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Other records listing Gish Biomedical, Inc. as applicant

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Related Devices (Code: DQY)

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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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