510(k) K813331 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
P51 ANGIOPLASTY PRESSURE TRANSDUCER
| Applicant | Konigsberg Instruments, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 29, 1981 |
| Received | Nov 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813331
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.