FDA 510(k) Application Details - K133057

Device Classification Name	Percussor, Powered-Electric   More FDA Info for this Device
510(K) Number	K133057
Device Name	Percussor, Powered-Electric
Applicant	Westmed, Inc. 5580 S. NOGALES HIGHWAY TUCSON, AZ 85706 US Other 510(k) Applications for this Company
Contact	PAUL DRYDEN 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	09/27/2013
Decision Date	05/23/2014
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