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FDA 510(k)

MEDIZIV CENTRAL VEIN CATHETER

K-Number: K884491 · 1989-06-05

ApplicantMediziv Medical Devices, Ltd.
Decision Date1989-06-05
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDIZIV CENTRAL VEIN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Mediziv Medical Devices, Ltd.. It received FDA 510(k) clearance on 1989-06-05 under 510(k) number K884491. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIZIV CENTRAL VEIN CATHETER?

MEDIZIV CENTRAL VEIN CATHETER is a medical device that received FDA 510(k) clearance on 1989-06-05. The listed applicant is Mediziv Medical Devices, Ltd.. The 510(k) number is K884491.

When did MEDIZIV CENTRAL VEIN CATHETER receive FDA 510(k) clearance?

MEDIZIV CENTRAL VEIN CATHETER received FDA 510(k) clearance on 1989-06-05, under 510(k) number K884491.

Who is the listed applicant for MEDIZIV CENTRAL VEIN CATHETER?

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

What is the FDA product code for MEDIZIV CENTRAL VEIN CATHETER?

The FDA product code for MEDIZIV CENTRAL VEIN CATHETER is DQY.

Related Clinical Trials

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.

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Other records listing Mediziv Medical Devices, Ltd. 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.

K894725MEDIZIV EPIDURAL SYSTEMS

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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