DUPEL IONTOPHORESIS DEVICE— 510(k) K915444
Substantially EquivalentEmpi
FDA 510(k) clearance K915444 for DUPEL IONTOPHORESIS DEVICE, Substantially Equivalent on 1994-07-15. Applicant: Empi.
Clearance details
- Applicant
- Empi
- Product code
- Code EGJ
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Arden Hills, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.