FDA 510(k) Application Details - K010184

Device Classification Name	Instrument, Manual, Surgical, General Use   More FDA Info for this Device
510(K) Number	K010184
Device Name	Instrument, Manual, Surgical, General Use
Applicant	CANICA DESIGN, INC. 36 MILL ST. ALMONTE, ONTARIO KOA1AO CA Other 510(k) Applications for this Company
Contact	GEORGETTE ROY Other 510(k) Applications for this Contact
Regulation Number	878.4800   More FDA Info for this Regulation Number
Classification Product Code	MDM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/19/2001
Decision Date	06/22/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review