FDA 510(k)

FIAB SPA, MODELS F7244, F7233, F7234, F7277

K-Number: K100333 · 2010-06-21

Decision Date2010-06-21

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

FIAB SPA, MODELS F7244, F7233, F7234, F7277 is the device name listed in this FDA 510(k) record. The listed applicant is Fiab Spa. It received FDA 510(k) clearance on 2010-06-21 under 510(k) number K100333. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIAB SPA, MODELS F7244, F7233, F7234, F7277?

FIAB SPA, MODELS F7244, F7233, F7234, F7277 is a medical device that received FDA 510(k) clearance on 2010-06-21. The listed applicant is Fiab Spa. The 510(k) number is K100333.

When did FIAB SPA, MODELS F7244, F7233, F7234, F7277 receive FDA 510(k) clearance?

FIAB SPA, MODELS F7244, F7233, F7234, F7277 received FDA 510(k) clearance on 2010-06-21, under 510(k) number K100333.

Who is the listed applicant for FIAB SPA, MODELS F7244, F7233, F7234, F7277?

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

What is the FDA product code for FIAB SPA, MODELS F7244, F7233, F7234, F7277?

The FDA product code for FIAB SPA, MODELS F7244, F7233, F7234, F7277 is GEI.

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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.