FDA 510(k) Application Details - K000507

Device Classification Name	Stimulator, Nerve   More FDA Info for this Device
510(K) Number	K000507
Device Name	Stimulator, Nerve
Applicant	UROMED CORP. 1400 PROVIDENCE HWY. NORWOOD, MA 02062 US Other 510(k) Applications for this Company
Contact	FREDERICK TOBIA Other 510(k) Applications for this Contact
Regulation Number	874.1820   More FDA Info for this Regulation Number
Classification Product Code	ETN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/15/2000
Decision Date	04/21/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review