FDA 510(k) Application Details - K023342

Device Classification Name	Stimulator, Nerve, Peripheral, Electric   More FDA Info for this Device
510(K) Number	K023342
Device Name	Stimulator, Nerve, Peripheral, Electric
Applicant	HDC CORP. 628 GIBRALTAR COURT MILPITAS, CA 95035 US Other 510(k) Applications for this Company
Contact	EARL SMART Other 510(k) Applications for this Contact
Regulation Number	868.2775   More FDA Info for this Regulation Number
Classification Product Code	KOI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/07/2002
Decision Date	03/02/2004
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