FDA 510(k) Application Details - K982889

Device Classification Name	Percussor, Powered-Electric   More FDA Info for this Device
510(K) Number	K982889
Device Name	Percussor, Powered-Electric
Applicant	ELECTROMED, INC. 14920 MINNETONKA IND. RD. MINNETONKA, MN 55345 US Other 510(k) Applications for this Company
Contact	CHET SIEVERT 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	08/17/1998
Decision Date	06/01/1999
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