FDA 510(k) Application Details - K965192

Device Classification Name	Percussor, Powered-Electric   More FDA Info for this Device
510(K) Number	K965192
Device Name	Percussor, Powered-Electric
Applicant	AMERICAN BIOSYSTEMS, INC. 1375 WOLTERS BLVD., SUITE 116 ST.PAUL, MN 55110 US Other 510(k) Applications for this Company
Contact	PHILLIP ROSE 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	12/24/1996
Decision Date	06/24/1997
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