510(k) K120846 ยท LIO Device, Specimen Collection
TRANSPORT CULTURE MEDIUM DEVICE
| Applicant | Puritan Medical Products, LLC, Guilford ME, US |
| Decision | Substantially Equivalent, Jun 8, 2012 |
| Received | Mar 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120846
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.