ClearanceBrief
510(k) K172751 ยท MQK Labware, Assisted Reproduction

iVitri Straw

ApplicantReprobitech Corp., Flushing NY, US
DecisionSubstantially Equivalent, Feb 9, 2018
ReceivedSep 12, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172751

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.