FDA 510(k) Application Details - K042113

Device Classification Name	Plethysmograph, Impedance   More FDA Info for this Device
510(K) Number	K042113
Device Name	Plethysmograph, Impedance
Applicant	NONINVASIVE MEDICAL TECHNOLOGIES, LLC. 4367 TUOLUMNE PLACE CARLSBAD, CA 92008 US Other 510(k) Applications for this Company
Contact	ALDEN KAY Other 510(k) Applications for this Contact
Regulation Number	870.2770   More FDA Info for this Regulation Number
Classification Product Code	DSB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/05/2004
Decision Date	09/14/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review