SMARTmatic
K-Number: K163239 · 2017-03-17
ApplicantKaltenbach & Voigt GmbH
Decision Date2017-03-17
Product CodeEFA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
SMARTmatic is a medical device manufactured by Kaltenbach & Voigt GmbH. It received FDA 510(k) clearance on 2017-03-17 under approval number K163239. The device is classified under product code EFA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SMARTmatic?
SMARTmatic is a medical device that received FDA 510(k) clearance on 2017-03-17. It is manufactured by Kaltenbach & Voigt GmbH. The 510(k) number is K163239.
When was SMARTmatic approved by the FDA?
SMARTmatic received FDA 510(k) clearance on 2017-03-17, under approval number K163239.
What company makes SMARTmatic?
SMARTmatic is manufactured by Kaltenbach & Voigt GmbH.
What is the FDA product code for SMARTmatic?
The FDA product code for SMARTmatic is EFA.
Other Devices by Kaltenbach & Voigt GmbH
Related Devices (Code: EFA)
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.