510(k) K150357 ยท NLH Catheter, Recording, Electrode, Reprocessed
Reprocessed Electrophysiology Diagnostic Catheters
| Applicant | Sterilmed, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Aug 27, 2015 |
| Received | Feb 12, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150357
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.