NeoWave Pain Relief and Recovery System, Model# T16-2020— 510(k) K202693
Substantially EquivalentEva Medtec, Inc.
FDA 510(k) clearance K202693 for NeoWave Pain Relief and Recovery System, Model# T16-2020, Substantially Equivalent on 2021-03-05. Applicant: Eva Medtec, Inc.. Device class: 2.
Clearance details
- Applicant
- Eva Medtec, Inc.
- Product code
- Code IRP
- Device class
- Class 2
- Regulation
- 21 CFR 890.5650
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bloomington, MN, US
Recent devices under product code IRP
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