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FDA 510(k)

RMI INTERNAL MAMMARY ARTERY CANNULA

K-Number: K960098 · 1996-03-26

ApplicantResearch Medical, Inc.
Decision Date1996-03-26
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RMI INTERNAL MAMMARY ARTERY 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 1996-03-26 under 510(k) number K960098. The device is classified under product code DQR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMI INTERNAL MAMMARY ARTERY CANNULA?

RMI INTERNAL MAMMARY ARTERY CANNULA is a medical device that received FDA 510(k) clearance on 1996-03-26. The listed applicant is Research Medical, Inc.. The 510(k) number is K960098.

When did RMI INTERNAL MAMMARY ARTERY CANNULA receive FDA 510(k) clearance?

RMI INTERNAL MAMMARY ARTERY CANNULA received FDA 510(k) clearance on 1996-03-26, under 510(k) number K960098.

Who is the listed applicant for RMI INTERNAL MAMMARY ARTERY 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 INTERNAL MAMMARY ARTERY CANNULA?

The FDA product code for RMI INTERNAL MAMMARY ARTERY CANNULA is DQR.

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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 SETK951344RMI HEMOCONCENTRATORK922083RMI SURGICCAL SITE VISUALIZATION WANDK920936RMI EXTERNAL CORONARY ARTERY OCCLUDER

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Related Devices (Code: DQR)

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.

K131446INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLESIntegra LifeSciences CorporationK07355918 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA IIEdwards Lifesciences Research MedicalK051655ANGIODYNAMICS, INC., MICRO ACCESS KITSAngioDynamics, Inc.K030398CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221Cardiacassist, Inc.K902674DATASCOPE ARTERIAL CANNULA W/ACCESS PORTDatascope Corp.K894784MODIFIED SHILEY FEMORAL VENOUS CANNULAShiley, 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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