FDA Approved Wellness Pro 2010

Classification Name: TENS device Transcutaneous Electrical Nerve Stimulator for Pain Relief CFR 882.5890,
Class II, Product Code 84GZJ (prescription) or Stimulator, Nerve, Transcutaneous for Pain Relief.

[PDF] 510(k) Summary
... RE: K062616 Trade/Device Name: Wellness Pro 2010 Regulation Number: 21 CFR 882.5890
Regulation Name: Transcutaneous electrical nerve stimulator for pain relief ...
www.fda.gov/cdrh/pdf6/K062616.pdf - 08-07-2007 - Text Version

FDA > CDRH > 510(k) Premarket Notification Database Search
... Device Classification Name, stimulator, nerve, transcutaneous, for pain relief.
510(k) Number, K062616. Device Name, WELLNESSPRO 2010. Applicant, ...
www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=22659 - Cached

US FDA/CDRH: 510(k)s Final Decisions Rendered for July 2007
510(k)s Final Decisions Rendered for July 2007
www.fda.gov/cdrh/510k/sumjul07.html - 12-13-2007 - Cached

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