510(k) K954422 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
PER-Q-CATH MID-LINE
| Applicant | Gesco Intl., Inc., Woburn MA, US |
| Decision | Substantially Equivalent, Dec 15, 1995 |
| Received | Sep 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954422
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.