Atlas FDA

VIBRAMETER

FDA 510(k) clearance K843486 · decided 1984-12-24

Clearance details

K-number
K843486
Device name
VIBRAMETER
Applicant
Somedic AB
Decision
Substantially Equivalent
Date received
1984-09-06
Decision date
1984-12-24
Days to decision
109 days
Clearance type
Traditional
Product code
LLN
Device class
1
Regulation number
882.1200
Medical specialty
Neurology
Advisory committee
Neurology
Location
Sweden, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PAIN VISION, MODEL PS-2100 (K072882)Osachi Co., Ltd.2009-01-08
VPT METER (K030829)Xilas Medical, Inc.2003-12-05
GSA GENITO SENSORY ANALYZER (K010981)Medoc Ltd. Advanced Medical Systems2001-09-20
MEDI-DX 7000 (K964622)Neuro-Diagnostic Assoc.1997-12-01
AP-4000, AIR PULSE SENSORY STIMULATOR (K964815)Pentax Precision Instrument Corp.1997-09-04
VSA 3000 VIBRATORYN SENSORY ANALYZER (K970180)Eare Consulting Service1997-04-25
NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 (K934368)Nk Biotechnical Engineering Co.1994-08-11
VIBROTACTILE TESTER, MODEL NO. VTT-100 (K921560)Topical Testing, Inc.1992-10-30
CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4 (K910624)Wr Medical Electronics Co.1992-01-17
TECA/MEDELEC TTT THERMAL THRESHOLD TESTER (K872931)Teca, Inc.1987-11-16
VIBRATRON II, VIBRATION SENSITIVITY TESTER (K863607)Sensortek, Inc.1986-12-03
NEUROMETER (K853608)Neurotron, Inc.1986-06-12

Recalls involving this device

No recalls on record reference this clearance.