510(k) K843383 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
MEDI-TECH DILATATION CATHETERS
| Applicant | Medi-Tech, Inc., Watertown MA, US |
| Decision | Substantially Equivalent, Oct 24, 1984 |
| Received | Aug 28, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843383
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.