510(k) K101789 ยท NLH Catheter, Recording, Electrode, Reprocessed
REPROCESSED ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Aug 19, 2010 |
| Received | Jun 28, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101789
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.