• 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 stimulator, nerve, transcutaneous, for pain relief
510(k) Number K173233
Device Name ReliefBand 1.5
ReliefBand Technologies
220 Gibraltar Rd Ste 270
horsham,  PA  19044
Applicant Contact dave hartman
Whitman Regulatory Consulting
616 Revere Court
flemington,  NJ  08822
Correspondent Contact barbara whitman
Regulation Number882.5890
Classification Product Code
Date Received10/05/2017
Decision Date 11/30/2017
Decision substantially equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No