510(k) K020728 ยท HCA Catheter, Ventricular
MIETHKE SHUNT SYSTEM
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 5, 2002 |
| Received | Mar 6, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020728
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 12, 2013 | Aesculap, Inc. Aesculap(R) - Miethke Shunt System, FT040T - Control Reservoir Set w/Distal Catheter and FT075P 0 Ventric Cathet, w/Stylet and RT-ANG Guide
Central Nervous System Shunt and Components intended to shu Terminated |
JXG | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.