510(k) K973305 · MDB System, Blood Culturing

BACT/ALERT CULTURE BOTTLES

Applicant	Organon Teknika Corp., Durham NC, US
Decision	Substantially Equivalent, Nov 17, 1997
Received	Sep 3, 1997
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K973305

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.