510(k) K170922 ยท NLH Catheter, Recording, Electrode, Reprocessed
Reprocessed Webster CS Bi-Directional Diagnostic EP Catheter, Reprocessed Webster CS Bi-Directional Diagnostic EP Catheter (with Auto ID)
| Applicant | Innovative Health, LLC, Scottsdale AZ, US |
| Decision | Substantially Equivalent, Jun 22, 2017 |
| Received | Mar 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170922
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.