510(k) K964777 · KNW Instrument, Biopsy

TZ

Applicant	Gallini Intl., Inc., Glen Allen VA, US
Decision	Substantially Equivalent, Jan 3, 1997
Received	Nov 27, 1996
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K964777

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.