MAZIC Claro CAD and MAZIC Claro Press
K-Number: K203672 · 2021-07-01
ApplicantVericom Co., Ltd.
Decision Date2021-07-01
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
MAZIC Claro CAD and MAZIC Claro Press is a medical device manufactured by Vericom Co., Ltd.. It received FDA 510(k) clearance on 2021-07-01 under approval number K203672. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MAZIC Claro CAD and MAZIC Claro Press?
MAZIC Claro CAD and MAZIC Claro Press is a medical device that received FDA 510(k) clearance on 2021-07-01. It is manufactured by Vericom Co., Ltd.. The 510(k) number is K203672.
When was MAZIC Claro CAD and MAZIC Claro Press approved by the FDA?
MAZIC Claro CAD and MAZIC Claro Press received FDA 510(k) clearance on 2021-07-01, under approval number K203672.
What company makes MAZIC Claro CAD and MAZIC Claro Press?
MAZIC Claro CAD and MAZIC Claro Press is manufactured by Vericom Co., Ltd..
What is the FDA product code for MAZIC Claro CAD and MAZIC Claro Press?
The FDA product code for MAZIC Claro CAD and MAZIC Claro Press is EIH.
Other Devices by Vericom Co., Ltd.
Related Devices (Code: EIH)
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.