ClearanceBrief
510(k) K170305 ยท FMJ Manometer, Spinal-Fluid

Spinal Manometer NRFit; Spinal Manometer LUER

ApplicantPAJUNK GmbH Medizintechnologie, Geisingen, DE
DecisionSubstantially Equivalent, Jul 25, 2017
ReceivedJan 31, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170305

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.