510(k) K011383 ยท ETD Tube, Tympanostomy
MICRODOSE CATH, MODELS 90121-201, -202, -203
| Applicant | Durect Corp., Cupertino CA, US |
| Decision | Substantially Equivalent, Jun 25, 2001 |
| Received | May 7, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011383
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.