ProMedTek Model C1400 Shortwave Diathermy Device— 510(k) K162240
Substantially EquivalentPromedtek, Inc.
FDA 510(k) clearance K162240 for ProMedTek Model C1400 Shortwave Diathermy Device, Substantially Equivalent on 2016-11-17. Applicant: Promedtek, Inc.. Device class: 2.
Clearance details
- Applicant
- Promedtek, Inc.
- Product code
- Code IMJ
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Scottsdale, AZ, US
Recent devices under product code IMJ
view allMore clearances from Promedtek, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.