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FDA 510(k)

QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS

K-Number: K951088 · 1995-06-14

ApplicantQuest Medical, Inc.
Decision Date1995-06-14
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS 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 1995-06-14 under 510(k) number K951088. 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 RETROGRADE CARDIPLEGIA CANNULA-RCCS?

QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS is a medical device that received FDA 510(k) clearance on 1995-06-14. The listed applicant is Quest Medical, Inc.. The 510(k) number is K951088.

When did QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS receive FDA 510(k) clearance?

QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS received FDA 510(k) clearance on 1995-06-14, under 510(k) number K951088.

Who is the listed applicant for QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS?

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 RETROGRADE CARDIPLEGIA CANNULA-RCCS?

The FDA product code for QUEST RETROGRADE CARDIPLEGIA CANNULA-RCCS 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.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, Inc.

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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