RUGALIFT, MODEL# V.2.1— 510(k) K071573
Substantially EquivalentFatrotek S.R.L.
FDA 510(k) clearance K071573 for RUGALIFT, MODEL# V.2.1, Substantially Equivalent on 2008-12-09. Applicant: Fatrotek S.R.L.. Device class: 2.
Clearance details
- Applicant
- Fatrotek S.R.L.
- Product code
- Code NFO
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Auvernier, CH
Recent devices under product code NFO
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