510(k) K974440 · KNW Instrument, Biopsy

IBI

Applicant	Gallini U.S., LLC, Richmond VA, US
Decision	Substantially Equivalent, Jan 30, 1998
Received	Nov 25, 1997
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K974440

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.