ClearanceBrief
510(k) K071573 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

RUGALIFT, MODEL# V.2.1

ApplicantFatrotek S.R.L., Auvernier, CH
DecisionSubstantially Equivalent, Dec 9, 2008
ReceivedJun 8, 2007
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K071573

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.