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FDA 510(k)

MEDICAN ALPHA

K-Number: K063469 · 2006-12-01

Decision Date2006-12-01
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDICAN ALPHA is the device name listed in this FDA 510(k) record. The listed applicant is Eastern Medikit , Ltd.. It received FDA 510(k) clearance on 2006-12-01 under 510(k) number K063469. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAN ALPHA?

MEDICAN ALPHA is a medical device that received FDA 510(k) clearance on 2006-12-01. The listed applicant is Eastern Medikit , Ltd.. The 510(k) number is K063469.

When did MEDICAN ALPHA receive FDA 510(k) clearance?

MEDICAN ALPHA received FDA 510(k) clearance on 2006-12-01, under 510(k) number K063469.

Who is the listed applicant for MEDICAN ALPHA?

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

What is the FDA product code for MEDICAN ALPHA?

The FDA product code for MEDICAN ALPHA is FOZ.

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: FOZ)

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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