510(k) K913842 ยท JXG Shunt, Central Nervous System And Components
CORDIS RIGHT-ANGLE CATHETER GUIDE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 19, 1992 |
| Received | Aug 28, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913842
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.