MODIFICATION TO:NESS L300— 510(k) K080219
Substantially EquivalentNess-Neuromuscular Electrical Stimulation Systems
FDA 510(k) clearance K080219 for MODIFICATION TO:NESS L300, Substantially Equivalent on 2008-02-28. Applicant: Ness-Neuromuscular Electrical Stimulation Systems.
Clearance details
- Applicant
- Ness-Neuromuscular Electrical Stimulation Systems
- Product code
- Code GZI
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Valencia, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.