510(k) K932993 · MFD Cannula, Intrauterine Insemination

INTRAUTERINE CATHETER AND INTRODUCER

Applicant	Conceptus, Inc., San Carlos CA, US
Decision	Substantially Equivalent, Jan 6, 1995
Received	Jun 18, 1993
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K932993

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.