510(k) K993913 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
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| Applicant | Infinity Extrusion & Engineering, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Aug 9, 2000 |
| Received | Nov 17, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993913
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.