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FDA 510(k), K910624, CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4
FDA 510(k), K910624, CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4
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510(K) Number: K910624
Device Name: CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4
Manufacturer: WR MEDICAL ELECTRONICS CO.
Device Classification Name: device, vibration threshold measurement
Regulation Number: 882.1200
Classification Product Code: LLN
Date Received: 02/12/1991
Decision Date: 01/17/1992
Regulation Medical Specialty: Neurology
Device Name: CASE IV COMPUTER AIDED SENSORY EVALUATOR VERSION 4
Manufacturer: WR MEDICAL ELECTRONICS CO.
Device Classification Name: device, vibration threshold measurement
Regulation Number: 882.1200
Classification Product Code: LLN
Date Received: 02/12/1991
Decision Date: 01/17/1992
Regulation Medical Specialty: Neurology
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