FDA 510(k) Application Details - K201490

Device Classification Name	Percussor, Powered-Electric   More FDA Info for this Device
510(K) Number	K201490
Device Name	Percussor, Powered-Electric
Applicant	Med Systems, Inc. 2631 Ariane Drive San Diego, CA 92117 US Other 510(k) Applications for this Company
Contact	Susan B Davis Other 510(k) Applications for this Contact
Regulation Number	868.5665   More FDA Info for this Regulation Number
Classification Product Code	BYI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/04/2020
Decision Date	02/12/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review