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FDA 510(k)

QUEST VEIN GRAFT PERFUSION SET

K-Number: K952531 · 1995-08-24

ApplicantQuest Medical, Inc.
Decision Date1995-08-24
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUEST VEIN GRAFT PERFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Quest Medical, Inc.. It received FDA 510(k) clearance on 1995-08-24 under 510(k) number K952531. 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 QUEST VEIN GRAFT PERFUSION SET?

QUEST VEIN GRAFT PERFUSION SET is a medical device that received FDA 510(k) clearance on 1995-08-24. The listed applicant is Quest Medical, Inc.. The 510(k) number is K952531.

When did QUEST VEIN GRAFT PERFUSION SET receive FDA 510(k) clearance?

QUEST VEIN GRAFT PERFUSION SET received FDA 510(k) clearance on 1995-08-24, under 510(k) number K952531.

Who is the listed applicant for QUEST VEIN GRAFT PERFUSION SET?

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

What is the FDA product code for QUEST VEIN GRAFT PERFUSION SET?

The FDA product code for QUEST VEIN GRAFT PERFUSION SET is DTL.

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Related Devices (Code: DTL)

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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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