510(k) K000135 · KNW Instrument, Biopsy

PRO.DUCT CATHETER, MODEL CTH03

Applicant	Pro. Duct Health, Inc., Menlo Park CA, US
Decision	Substantially Equivalent, Apr 10, 2000
Received	Jan 18, 2000
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K000135

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.