LLN · Class I · 21 CFR 882.1200

FDA Product Code LLN: Device, Vibration Threshold Measurement

Leading manufacturers include Medoc Ltd. Advanced Medical Systems, Osachi Co., Ltd. and Teca, Inc..

13
Total
13
Cleared
240d
Avg days
1984
Since

FDA 510(k) Cleared Device, Vibration Threshold Measurement Devices (Product Code LLN)

13 devices
1–13 of 13
Cleared Jan 08, 2009
PAIN VISION, MODEL PS-2100
K072882
Osachi Co., Ltd.
Neurology · 457d
Cleared Sep 20, 2001
GSA GENITO SENSORY ANALYZER
K010981
Medoc Ltd. Advanced Medical Systems
Neurology · 171d
Cleared Dec 01, 1997
MEDI-DX 7000
K964622
Neuro-Diagnostic Assoc.
Neurology · 378d
Cleared Sep 04, 1997
AP-4000, AIR PULSE SENSORY STIMULATOR
K964815
Pentax Precision Instrument Corp.
Neurology · 279d
Cleared Apr 25, 1997
VSA 3000 VIBRATORYN SENSORY ANALYZER
K970180
Eare Consulting Service
Neurology · 98d
Cleared Nov 16, 1987
TECA/MEDELEC TTT THERMAL THRESHOLD TESTER
K872931
Teca, Inc.
Neurology · 112d

About Product Code LLN - Regulatory Context