FDA 510(k) Application Details - K972859

Device Classification Name	Percussor, Powered-Electric   More FDA Info for this Device
510(K) Number	K972859
Device Name	Percussor, Powered-Electric
Applicant	BRADSTREET CLINICAL RESEARCH ASSOC., INC. 1588 ROUTE 130 NORTH SUITE C-2 NORTH BRUNSWICK, NJ 08902 US Other 510(k) Applications for this Company
Contact	PATRICIA W BRADSTREET 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	08/04/1997
Decision Date	06/05/1998
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