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FDA 510(k)

7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM

K-Number: K880776 · 1988-05-02

ApplicantMedsurg Industries, Inc.
Decision Date1988-05-02
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1988-05-02 under 510(k) number K880776. 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 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM?

7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM is a medical device that received FDA 510(k) clearance on 1988-05-02. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K880776.

When did 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM receive FDA 510(k) clearance?

7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM received FDA 510(k) clearance on 1988-05-02, under 510(k) number K880776.

Who is the listed applicant for 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM?

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

What is the FDA product code for 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM?

The FDA product code for 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM is DQR.

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Other records listing Medsurg Industries, 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.

K920780MEDSURG INSERTION TRAYK940175MEDSURG STERILE O.R. TOWELSK934731MEDSURG STERILE IMAGING PRODUCTSK925558INFILTUBEK934971STERILE LAPAROTOMY SPONGESK920421MEDSURG MARSHMALLOW TRAY

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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.K960098RMI INTERNAL MAMMARY ARTERY CANNULAResearch Medical, Inc.K902674DATASCOPE ARTERIAL CANNULA W/ACCESS PORTDatascope Corp.

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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