510(k) K883607 ยท GYK Instrument, Shunt System Implantation
PEEL-AWAY INTRODUCER FOR VENTRICULAR CATHETER
| Applicant | Codman & Shurtleff, Inc., Randolph MA, US |
| Decision | Substantially Equivalent, Sep 30, 1988 |
| Received | Aug 23, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883607
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.