FDA 510(k) Application Details - K101723

Device Classification Name	Chair, Positioning, Electric   More FDA Info for this Device
510(K) Number	K101723
Device Name	Chair, Positioning, Electric
Applicant	DESIGN SPECIFIC FLETCHER UNIT 10 CABURN ENTERPRISE PARK THE BROYLE RINGMER EAST SUSSEX BN8 5NP GB Other 510(k) Applications for this Company
Contact	RICHARD FLETCHER Other 510(k) Applications for this Contact
Regulation Number	890.3110   More FDA Info for this Regulation Number
Classification Product Code	INO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/18/2010
Decision Date	12/23/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review