ParaMotion— 510(k) K203761
Substantially EquivalentPowerbasetec GmbH
FDA 510(k) clearance K203761 for ParaMotion, Substantially Equivalent on 2022-01-21. Applicant: Powerbasetec GmbH. Device class: 2.
Clearance details
- Applicant
- Powerbasetec GmbH
- Product code
- Code IPL
- Device class
- Class 2
- Regulation
- 21 CFR 890.3900
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bodensee, DE
Recent devices under product code IPL
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