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FDA 510(k)

QUEST CORONARY SINUS PERFUSION CANNULA -FRCC

K-Number: K941916 · 1995-04-06

ApplicantQuest Medical, Inc.
Decision Date1995-04-06
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUEST CORONARY SINUS PERFUSION CANNULA -FRCC 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 1995-04-06 under 510(k) number K941916. 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 CORONARY SINUS PERFUSION CANNULA -FRCC?

QUEST CORONARY SINUS PERFUSION CANNULA -FRCC is a medical device that received FDA 510(k) clearance on 1995-04-06. The listed applicant is Quest Medical, Inc.. The 510(k) number is K941916.

When did QUEST CORONARY SINUS PERFUSION CANNULA -FRCC receive FDA 510(k) clearance?

QUEST CORONARY SINUS PERFUSION CANNULA -FRCC received FDA 510(k) clearance on 1995-04-06, under 510(k) number K941916.

Who is the listed applicant for QUEST CORONARY SINUS PERFUSION CANNULA -FRCC?

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 CORONARY SINUS PERFUSION CANNULA -FRCC?

The FDA product code for QUEST CORONARY SINUS PERFUSION CANNULA -FRCC 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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