MED SCULPT— 510(k) K053041
Substantially EquivalentGeneral Project S.R.L.
FDA 510(k) clearance K053041 for MED SCULPT, Substantially Equivalent on 2006-08-02. Applicant: General Project S.R.L.. Device class: 2.
Clearance details
- Applicant
- General Project S.R.L.
- Product code
- Code IMI
- Device class
- Class 2
- Regulation
- 21 CFR 890.5300
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Reading, MA, US
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