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..
Clearance details
- Applicant
- Fatrotek S.R.L.
- Product code
- Code NFO
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Auvernier, CH
Data sourced from openFDA. This site is unofficial and independent of the FDA.