510(k) K202433 ยท PON Catheter, Balloon, Dilation Of Cervical Canal
Aqueduct 200 Cervical Dilation Balloon Catheter
| Applicant | Gtimd, LLC, Amherst NH, US |
| Decision | Substantially Equivalent, Oct 15, 2021 |
| Received | Aug 25, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202433
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.