FDA 510(k) Application Details - K960081

Device Classification Name	Light Source, Incandescent, Diagnostic   More FDA Info for this Device
510(K) Number	K960081
Device Name	Light Source, Incandescent, Diagnostic
Applicant	MITSUBISHI CABLE AMERICA, INC. 10551 WULFF DR. ORANGE, CA 92667 US Other 510(k) Applications for this Company
Contact	RONALD J EHMSEN Other 510(k) Applications for this Contact
Regulation Number	876.1500   More FDA Info for this Regulation Number
Classification Product Code	FCQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/11/1996
Decision Date	03/12/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review