510(k) K242003 ยท JXG Shunt, Central Nervous System And Components
XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Dec 16, 2024 |
| Received | Jul 9, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242003
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.