FDA 510(k)

HUMERAL HEAD, MANUAL DRIVER

K-Number: K062422 · 2006-11-07

Decision Date2006-11-07

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HUMERAL HEAD, MANUAL DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Vidacare Corporation. It received FDA 510(k) clearance on 2006-11-07 under 510(k) number K062422. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMERAL HEAD, MANUAL DRIVER?

HUMERAL HEAD, MANUAL DRIVER is a medical device that received FDA 510(k) clearance on 2006-11-07. The listed applicant is Vidacare Corporation. The 510(k) number is K062422.

When did HUMERAL HEAD, MANUAL DRIVER receive FDA 510(k) clearance?

HUMERAL HEAD, MANUAL DRIVER received FDA 510(k) clearance on 2006-11-07, under 510(k) number K062422.

Who is the listed applicant for HUMERAL HEAD, MANUAL DRIVER?

The FDA 510(k) record lists Vidacare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUMERAL HEAD, MANUAL DRIVER?

The FDA product code for HUMERAL HEAD, MANUAL DRIVER is FMI.

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Other records listing Vidacare Corporation as applicant

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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.