Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name Device, Vibration Threshold Measurement
510(k) Number K921560
Device Name VIBROTACTILE TESTER, MODEL NO. VTT-100
Applicant
Topical Testing, Inc.
1308 S. 1700 E., #209
Salt Lake City,  UT  84108
Applicant Contact ROBERT P TUCKETT
Correspondent
Topical Testing, Inc.
1308 S. 1700 E., #209
Salt Lake City,  UT  84108
Correspondent Contact ROBERT P TUCKETT
Regulation Number882.1200
Classification Product Code
LLN  
Date Received04/01/1992
Decision Date 10/30/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-