ClearanceBrief
510(k) K951644 ยท LWF Dilator, Nasal

ACUTEK'S CLEARPASSAGE

ApplicantAcutek Adhesive Specialties, Inc., Inglewood CA, US
DecisionSubstantially Equivalent, Jul 3, 1995
ReceivedApr 10, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951644

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.