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FDA 510(k)

QUEST VESSEL CATHETER

K-Number: K971928 · 1997-11-06

ApplicantQuest Medical, Inc.
Decision Date1997-11-06
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUEST VESSEL CATHETER 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 1997-11-06 under 510(k) number K971928. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUEST VESSEL CATHETER?

QUEST VESSEL CATHETER is a medical device that received FDA 510(k) clearance on 1997-11-06. The listed applicant is Quest Medical, Inc.. The 510(k) number is K971928.

When did QUEST VESSEL CATHETER receive FDA 510(k) clearance?

QUEST VESSEL CATHETER received FDA 510(k) clearance on 1997-11-06, under 510(k) number K971928.

Who is the listed applicant for QUEST VESSEL CATHETER?

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 VESSEL CATHETER?

The FDA product code for QUEST VESSEL CATHETER is DWF.

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Related Devices (Code: DWF)

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

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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