Multifrax Laser System— 510(k) K213332
Substantially EquivalentParadigm Medical Corporation
FDA 510(k) clearance K213332 for Multifrax Laser System, Substantially Equivalent on 2022-06-03. Applicant: Paradigm Medical Corporation. Device class: 2.
Clearance details
- Applicant
- Paradigm Medical Corporation
- Product code
- Product code ONG
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code ONG
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