DIGI-PRO TENS, MODEL WL-2204 AND WL-2205— 510(k) K020314
Substantially EquivalentWell-Life Healthcare, Inc.
FDA 510(k) clearance K020314 for DIGI-PRO TENS, MODEL WL-2204 AND WL-2205, Substantially Equivalent on 2002-04-30. Applicant: Well-Life Healthcare, Inc..
Clearance details
- Applicant
- Well-Life Healthcare, Inc.
- Product code
- Code IPF
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taichung, R.O.C., TW
Data sourced from openFDA. This site is unofficial and independent of the FDA.