FDA 510(k)

F20

K-Number: K103433 · 2011-01-03

Decision Date2011-01-03

Product CodeNDN

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

F20 is the device name listed in this FDA 510(k) record. The listed applicant is Teknimed, S.A.. It received FDA 510(k) clearance on 2011-01-03 under 510(k) number K103433. The device is classified under product code NDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the F20?

F20 is a medical device that received FDA 510(k) clearance on 2011-01-03. The listed applicant is Teknimed, S.A.. The 510(k) number is K103433.

When did F20 receive FDA 510(k) clearance?

F20 received FDA 510(k) clearance on 2011-01-03, under 510(k) number K103433.

Who is the listed applicant for F20?

The FDA 510(k) record lists Teknimed, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F20?

The FDA product code for F20 is NDN.

Other records listing Teknimed, S.A. 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.