510(k) K820520 · LIO Device, Specimen Collection

VD ALERT

Applicant	Intl. Research Distributors, Inc., Mchenry IL, US
Decision	Substantially Equivalent, May 14, 1982
Received	Feb 26, 1982
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K820520

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.