FDA 510(k) Application Details - K970763

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K970763
Device Name	Oximeter
Applicant	MEDICAL DATA ELECTRONICS 12720 WENTWORTH ST. ARLETA, CA 91331 US Other 510(k) Applications for this Company
Contact	DAVID M TRUEBLOOD Other 510(k) Applications for this Contact
Regulation Number	870.2700   More FDA Info for this Regulation Number
Classification Product Code	DQA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/03/1997
Decision Date	07/14/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review