FDA 510(k) Application Details - K955500

Device Classification Name	Arthroscope   More FDA Info for this Device
510(K) Number	K955500
Device Name	Arthroscope
Applicant	FUTURE MEDICAL SYSTEMS, INC. 205 EAST 63RD ST. SUITE 7A NEW YORK CITY, NY 10021 US Other 510(k) Applications for this Company
Contact	PATRICK JANIN Other 510(k) Applications for this Contact
Regulation Number	888.1100   More FDA Info for this Regulation Number
Classification Product Code	HRX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/01/1995
Decision Date	02/05/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review