510(k) K982929 ยท LWF Dilator, Nasal
MAXAIR NASAL DILATOR SYSTEM
| Applicant | Hnl Technologies, San Mateo CA, US |
| Decision | Substantially Equivalent, Sep 9, 1998 |
| Received | Aug 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982929
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.