FDA 510(k) Application Details - K960058

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K960058
Device Name	Oximeter
Applicant	BCI INTL., INC. W238 N1650 ROCKWOOD DR. WAUKESHA, WI 53188 US Other 510(k) Applications for this Company
Contact	DONALD J ALEXANDER 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	01/02/1996
Decision Date	05/15/1996
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