510(k) K172737 ยท LRC Instrument, Ent Manual Surgical
MESIRE - Balloon Sinus Dilatation System
| Applicant | M/S. Meril Life Sciences Private Limited, Chala, Vapi, IN |
| Decision | Substantially Equivalent, Dec 12, 2017 |
| Received | Sep 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172737
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.