510(k) K792639 ยท GYK Instrument, Shunt System Implantation
H-H SHUNT INTRODUCER
| Applicant | Holter-Hausner Intl., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 31, 1979 |
| Received | Dec 20, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792639
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.