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FDA 510(k)

REGIONAL ANAESTHESIA TRAY

K-Number: K932614 · 1994-09-21

Decision Date1994-09-21
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REGIONAL ANAESTHESIA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Mediziv Medical Products , Ltd.. It received FDA 510(k) clearance on 1994-09-21 under 510(k) number K932614. 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 REGIONAL ANAESTHESIA TRAY?

REGIONAL ANAESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1994-09-21. The listed applicant is Mediziv Medical Products , Ltd.. The 510(k) number is K932614.

When did REGIONAL ANAESTHESIA TRAY receive FDA 510(k) clearance?

REGIONAL ANAESTHESIA TRAY received FDA 510(k) clearance on 1994-09-21, under 510(k) number K932614.

Who is the listed applicant for REGIONAL ANAESTHESIA TRAY?

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

What is the FDA product code for REGIONAL ANAESTHESIA TRAY?

The FDA product code for REGIONAL ANAESTHESIA TRAY is CAZ.

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.

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.

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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