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FDA 510(k)

MEDIZIV EPIDURAL SYSTEMS

K-Number: K894725 · 1989-10-13

ApplicantMediziv Medical Devices, Ltd.
Decision Date1989-10-13
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIZIV EPIDURAL SYSTEMS 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 1989-10-13 under 510(k) number K894725. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIZIV EPIDURAL SYSTEMS?

MEDIZIV EPIDURAL SYSTEMS is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Mediziv Medical Devices, Ltd.. The 510(k) number is K894725.

When did MEDIZIV EPIDURAL SYSTEMS receive FDA 510(k) clearance?

MEDIZIV EPIDURAL SYSTEMS received FDA 510(k) clearance on 1989-10-13, under 510(k) number K894725.

Who is the listed applicant for MEDIZIV EPIDURAL SYSTEMS?

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 EPIDURAL SYSTEMS?

The FDA product code for MEDIZIV EPIDURAL SYSTEMS is CAZ.

Related Clinical Trials

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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.

K884491MEDIZIV CENTRAL VEIN CATHETER

Related Devices (Code: CAZ)

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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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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