PMD-2000 INTERFERENTIAL STIMULATOR— 510(k) K042881
Substantially EquivalentPhoenix Medical Devices, LLC
FDA 510(k) clearance K042881 for PMD-2000 INTERFERENTIAL STIMULATOR, Substantially Equivalent on 2004-11-18. Applicant: Phoenix Medical Devices, LLC. Device class: 2.
Clearance details
- Applicant
- Phoenix Medical Devices, LLC
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Newport Beach, CA, US
Recent devices under product code IPF
view allData sourced from openFDA. This site is unofficial and independent of the FDA.