FDA 510(k) Application Details - K001770

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K001770
Device Name	Oximeter
Applicant	BCI, INC. N7 W22025 JOHNSON RD. WAUKESHA, WI 53186 US Other 510(k) Applications for this Company
Contact	DONALD 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	06/12/2000
Decision Date	07/05/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review