FDA 510(k) Applications for Medical Device Product Code: LLN (Device, Vibration Threshold Measurement)

FDA 510(k) Applications for Medical Device Product Code "LLN"
(Device, Vibration Threshold Measurement)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K970180	EARE CONSULTING SERVICE	VSA 3000 VIBRATORYN SENSORY ANALYZER	04/25/1997
K010981	MEDOC LTD. ADVANCED MEDICAL SYSTEMS	GSA GENITO SENSORY ANALYZER	09/20/2001
K964622	NEURO-DIAGNOSTIC ASSOC.	MEDI-DX 7000	12/01/1997
K072882	OSACHI CO., LTD.	PAIN VISION, MODEL PS-2100	01/08/2009
K964815	PENTAX PRECISION INSTRUMENT CORP.	AP-4000, AIR PULSE SENSORY STIMULATOR	09/04/1997
K030829	XILAS MEDICAL, INC.	VPT METER	12/05/2003