FDA 510(k) Application Details - K983900

Device Classification Name	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic   More FDA Info for this Device
510(K) Number	K983900
Device Name	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Applicant	ADVANCED MEDICAL TECHNOLOGY LTD. 9712 S. ALTAMONT DR. SANDY, UT US Other 510(k) Applications for this Company
Contact	WILLIAM E MCKAY Other 510(k) Applications for this Contact
Regulation Number	870.2780   More FDA Info for this Regulation Number
Classification Product Code	JOM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/03/1998
Decision Date	01/29/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review