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FDA 510(k)

RMI VENOUS DRAINAGE CANNULA

K-Number: K870109 · 1987-03-16

ApplicantResearch Medical, Inc.
Decision Date1987-03-16
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RMI VENOUS DRAINAGE CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Research Medical, Inc.. It received FDA 510(k) clearance on 1987-03-16 under 510(k) number K870109. 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 RMI VENOUS DRAINAGE CANNULA?

RMI VENOUS DRAINAGE CANNULA is a medical device that received FDA 510(k) clearance on 1987-03-16. The listed applicant is Research Medical, Inc.. The 510(k) number is K870109.

When did RMI VENOUS DRAINAGE CANNULA receive FDA 510(k) clearance?

RMI VENOUS DRAINAGE CANNULA received FDA 510(k) clearance on 1987-03-16, under 510(k) number K870109.

Who is the listed applicant for RMI VENOUS DRAINAGE CANNULA?

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

What is the FDA product code for RMI VENOUS DRAINAGE CANNULA?

The FDA product code for RMI VENOUS DRAINAGE CANNULA is DWF.

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Other records listing Research Medical, Inc. as applicant

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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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