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FDA 510(k)

FIT TEST C&B

K-Number: K110050 · 2011-03-28

ApplicantVoco GmbH
Decision Date2011-03-28
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIT TEST C&B is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2011-03-28 under 510(k) number K110050. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIT TEST C&B?

FIT TEST C&B is a medical device that received FDA 510(k) clearance on 2011-03-28. The listed applicant is Voco GmbH. The 510(k) number is K110050.

When did FIT TEST C&B receive FDA 510(k) clearance?

FIT TEST C&B received FDA 510(k) clearance on 2011-03-28, under 510(k) number K110050.

Who is the listed applicant for FIT TEST C&B?

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

What is the FDA product code for FIT TEST C&B?

The FDA product code for FIT TEST C&B is ELW.

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Related Devices (Code: ELW)

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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.

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