IontoDC— 510(k) K170291
Substantially EquivalentSoterix Medical, Inc.
FDA 510(k) clearance K170291 for IontoDC, Substantially Equivalent on 2017-05-01. Applicant: Soterix Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Soterix Medical, Inc.
- Product code
- Code EGJ
- Device class
- Class 2
- Regulation
- 21 CFR 890.5525
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
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