510(k) K220611 · KNW Instrument, Biopsy

SUREcore Plus Biopsy Instrument

Applicant	Uro-1, Inc., Greensboro NC, US
Decision	Substantially Equivalent, Dec 2, 2022
Received	Mar 3, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K220611

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.