ART-Plan+ (v.3.0.0)— 510(k) K242822
Substantially EquivalentTherapanacea Sas
FDA 510(k) clearance K242822 for ART-Plan+ (v.3.0.0), Substantially Equivalent on 2025-02-25. Applicant: Therapanacea Sas. Device class: 2.
Clearance details
- Applicant
- Therapanacea Sas
- Product code
- Code MUJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paris, FR
Recent devices under product code MUJ
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