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FDA 510(k)

RMI ANTEPLEGIA CANNULA

K-Number: K896636 · 1990-02-15

ApplicantResearch Medical, Inc.
Decision Date1990-02-15
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RMI ANTEPLEGIA 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 1990-02-15 under 510(k) number K896636. 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 ANTEPLEGIA CANNULA?

RMI ANTEPLEGIA CANNULA is a medical device that received FDA 510(k) clearance on 1990-02-15. The listed applicant is Research Medical, Inc.. The 510(k) number is K896636.

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

RMI ANTEPLEGIA CANNULA received FDA 510(k) clearance on 1990-02-15, under 510(k) number K896636.

Who is the listed applicant for RMI ANTEPLEGIA 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 ANTEPLEGIA CANNULA?

The FDA product code for RMI ANTEPLEGIA CANNULA is DWF.

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Other records listing Research Medical, Inc. as applicant

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.

K970739RMI HEMOCONCENTRATOR PREFERENCE PACKK964833RMI DUAL FLUID IRRIGATING SYRINGEK961927RMI HEMOCONCENTRACTOR TUBING SETK960098RMI INTERNAL MAMMARY ARTERY CANNULAK951344RMI HEMOCONCENTRATORK922083RMI SURGICCAL SITE VISUALIZATION WAND

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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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