ClearanceBrief
510(k) K930124 ยท KXH Cradle, Patient, Radiologic

VARIANT OF OCTOSTOP AND OCTOPAQUE

ApplicantOctostop, Inc., Montreal, Qc., CA
DecisionSubstantially Equivalent, Feb 9, 1994
ReceivedJan 12, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930124

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.