FDA 510(k), K921560, VIBROTACTILE TESTER, MODEL NO. VTT-100
FDA 510(k), K921560, VIBROTACTILE TESTER, MODEL NO. VTT-100
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510(K) Number: K921560
Device Name: VIBROTACTILE TESTER, MODEL NO. VTT-100
Manufacturer: TOPICAL TESTING, INC.
Device Classification Name: device, vibration threshold measurement
Regulation Number: 882.1200
Classification Product Code: LLN
Date Received: 04/01/1992
Decision Date: 10/30/1992
Regulation Medical Specialty: Neurology
Device Name: VIBROTACTILE TESTER, MODEL NO. VTT-100
Manufacturer: TOPICAL TESTING, INC.
Device Classification Name: device, vibration threshold measurement
Regulation Number: 882.1200
Classification Product Code: LLN
Date Received: 04/01/1992
Decision Date: 10/30/1992
Regulation Medical Specialty: Neurology
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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