FDA 510(k) Application Details - K231591

Device Classification Name	More FDA Info for this Device
510(K) Number	K231591
Device Name	V-Print c&b temp
Applicant	VOCO GmbH Anton-Flettner-Str. 1-3 Cuxhaven 27472 DE Other 510(k) Applications for this Company
Contact	Sarah Schaudel Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	POW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/01/2023
Decision Date	07/31/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review