ClearanceBrief
510(k) K083208 ยท MRX System, Assisted Reproduction Laser

SATURN ACTIVE LASER SYSTEM

ApplicantResearch Instruments , Ltd., Falmouth, Cornwall, GB
DecisionSubstantially Equivalent, Aug 25, 2009
ReceivedOct 31, 2008
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K083208

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.