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
K853608 NEUROTRON, INC. NEUROMETER 06/12/1986
K934368 NK BIOTECHNICAL ENGINEERING CO. NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 08/11/1994
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
K863607 SENSORTEK, INC. VIBRATRON II, VIBRATION SENSITIVITY TESTER 12/03/1986
K843486 SOMEDIC AB VIBRAMETER 12/24/1984
K872931 TECA, INC. TECA/MEDELEC TTT THERMAL THRESHOLD TESTER 11/16/1987
K921560 TOPICAL TESTING, INC. VIBROTACTILE TESTER, MODEL NO. VTT-100 10/30/1992
K910624 WR MEDICAL ELECTRONICS CO. CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 01/17/1992
K030829 XILAS MEDICAL, INC. VPT METER 12/05/2003


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact