Registrado Scan
K-Number: K171815 · 2017-11-15
ApplicantVoco GmbH
Decision Date2017-11-15
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Registrado Scan is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2017-11-15 under approval number K171815. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Registrado Scan?
Registrado Scan is a medical device that received FDA 510(k) clearance on 2017-11-15. It is manufactured by Voco GmbH. The 510(k) number is K171815.
When was Registrado Scan approved by the FDA?
Registrado Scan received FDA 510(k) clearance on 2017-11-15, under approval number K171815.
What company makes Registrado Scan?
Registrado Scan is manufactured by Voco GmbH.
What is the FDA product code for Registrado Scan?
The FDA product code for Registrado Scan is EBF.
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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.