ClearanceBrief
510(k) K880991 ยท HHR Laser, Surgical, Gynecologic

LASER OPTICAL CATHETER SYSTEM

ApplicantMedline Industries, Inc., Englewood CO, US
DecisionSubstantially Equivalent, May 25, 1988
ReceivedMar 8, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880991

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.