FDA 510(k) Application Details - K213814

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K213814
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	Viveve, Inc. 345 Inverness Drive South, Building B, Suite 250 Englewood, CO 80112 US Other 510(k) Applications for this Company
Contact	Kevin Robison Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/07/2021
Decision Date	02/02/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review