510(k) K030109 ยท NLH Catheter, Recording, Electrode, Reprocessed
ELECTROPHYSIOLOGY CATHETER
| Applicant | Alliance Medical Corp., Phoenix AZ, US |
| Decision | Substantially Equivalent, Aug 8, 2003 |
| Received | Jan 13, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030109
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 18, 2013 | Stryker Sustainability Solutions Reprocessed Diagnostic Electrophysiology (EP) Catheters and Diagnostic EP Catheter Cables, Model Numbers: D6-DR-252-RT, F6-QF-252RT, 201101, 201104, 401442, 401860, D7-A20-131-RT, 401661, 401972, 4019 Terminated |
NLH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.