510(k) K002139 ยท LTX Discs, Elution
ETEST LINEZOLID
| Applicant | Ab Biodisk, Solna, SE |
| Decision | Substantially Equivalent, Nov 8, 2000 |
| Received | Jul 17, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002139
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.