510(k) K051042 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
METRICATH GEMINI-P BALLOON CATHETER, MODELS RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, METRICATH CONSOLE, MODEL 1000
| Applicant | Angiometrx, Inc., Vancouver, Bc, CA |
| Decision | Substantially Equivalent, Aug 5, 2005 |
| Received | Apr 25, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051042
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.