ClearanceBrief
510(k) K810660 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

KREMER CORNEOMETER ULTRASONIC PACHOMETER

ApplicantAccutome, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 21, 1981
ReceivedMar 11, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810660

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.