Vibrotactile Tester, Model No. VTT-100
FDA 510(k) K921560 · Topical Testing, Inc.
510(k) numberK921560
Submission
- Device name
- Vibrotactile Tester, Model No. VTT-100
- Applicant
- Topical Testing, Inc.
Salt Lake City, UT, US - Received
- April 1, 1992
- Decision date
- October 30, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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Questions and answers
When was Vibrotactile Tester, Model No. VTT-100 cleared by the FDA?
Vibrotactile Tester, Model No. VTT-100 (K921560) received a 510(k) decision of Substantially Equivalent on October 30, 1992, 212 days after the submission was received.
What is the product code of K921560?
The FDA product code is LLN – Device, Vibration Threshold Measurement, a Class I (low risk) device regulated under 21 CFR 882.1200.