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FDA 510(k)

HARBOR CENTRAL VENOUS CATHETER

K-Number: K881884 · 1988-07-28

ApplicantHarbor Medical Devices, Inc.
Decision Date1988-07-28
Product CodeDQR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HARBOR CENTRAL VENOUS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Harbor Medical Devices, Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K881884. 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 HARBOR CENTRAL VENOUS CATHETER?

HARBOR CENTRAL VENOUS CATHETER is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Harbor Medical Devices, Inc.. The 510(k) number is K881884.

When did HARBOR CENTRAL VENOUS CATHETER receive FDA 510(k) clearance?

HARBOR CENTRAL VENOUS CATHETER received FDA 510(k) clearance on 1988-07-28, under 510(k) number K881884.

Who is the listed applicant for HARBOR CENTRAL VENOUS CATHETER?

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

What is the FDA product code for HARBOR CENTRAL VENOUS CATHETER?

The FDA product code for HARBOR CENTRAL VENOUS CATHETER is DQR.

Related Clinical Trials

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Other records listing Harbor Medical Devices, 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.

K884628HARBORIN CENTRAL VENOUS CATHETERK890518SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEMK882657HARBOR S.E.A.-PORT SURGICAL ACCESSORY KITK882190S.E.A.-PORT(TM) VASCULAR ACCESS SYSTEMK880297SEA - PORT INFUSION SETK874414HYPODERMIC NEEDLES, SINGLE LUMEN

View all 7 devices →

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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