FDA 510(k) Application Details - K201184

Device Classification Name	Material, Impression   More FDA Info for this Device
510(K) Number	K201184
Device Name	Material, Impression
Applicant	Lascod Spa Via Longo, 18 Sesto Fiorentino 50019 IT Other 510(k) Applications for this Company
Contact	Gualtiero Cozzi Other 510(k) Applications for this Contact
Regulation Number	872.3660   More FDA Info for this Regulation Number
Classification Product Code	ELW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/01/2020
Decision Date	05/05/2020
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review