510(k) K013820 ยท KXF Applicator, Absorbent Tipped, Non-Sterile
FINN CHAMBER (R)
| Applicant | Epitest Ltd. OY, Petaluma CA, US |
| Decision | Substantially Equivalent, Jan 30, 2002 |
| Received | Nov 16, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013820
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.