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FDA 510(k)

BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER

K-Number: K874618 · 1988-01-19

ApplicantBentley Laboratories, Inc.
Decision Date1988-01-19
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K874618. 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 BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER?

BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K874618.

When did BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1988-01-19, under 510(k) number K874618.

Who is the listed applicant for BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER?

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

What is the FDA product code for BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER?

The FDA product code for BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER is DQR.

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Other records listing Bentley Laboratories, 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.

K931967HE-30 GOLDK913956BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30K913692VENOUS RESERVOIR BAG MODEL NO. BMR-250(TM)K903641QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000QK894826UNIVOX W/HOLDERS, MODELS UNIVOX-HL, HLB, HLFK874867CATR(TM)-H CARDIOTOMY HOLDER

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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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