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FDA 510(k)

FUTURA

K-Number: K102524 · 2011-11-03

ApplicantDr. Oliver Wenker, M.D., M.B.A.
Decision Date2011-11-03
Product CodeIMG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FUTURA is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Oliver Wenker, M.D., M.B.A.. It received FDA 510(k) clearance on 2011-11-03 under 510(k) number K102524. The device is classified under product code IMG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUTURA?

FUTURA is a medical device that received FDA 510(k) clearance on 2011-11-03. The listed applicant is Dr. Oliver Wenker, M.D., M.B.A.. The 510(k) number is K102524.

When did FUTURA receive FDA 510(k) clearance?

FUTURA received FDA 510(k) clearance on 2011-11-03, under 510(k) number K102524.

Who is the listed applicant for FUTURA?

The FDA 510(k) record lists Dr. Oliver Wenker, M.D., M.B.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FUTURA?

The FDA product code for FUTURA is IMG.

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Related Devices (Code: IMG)

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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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