510(k) K864329 · KNW Instrument, Biopsy

MODELS 54601/54602/54603/54604 NEEDLE & BIOPSY KIT

Applicant	Dlp, Inc., Grand Rapids MI, US
Decision	Substantially Equivalent, Dec 3, 1986
Received	Nov 4, 1986
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K864329

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.