510(k) K832481 ยท HQX Implant, Orbital, Extra-Ocular
SCLERAL BUCKLING IMPLANTS DIF/TYPES
| Applicant | Storz Instrument Co., Walker MI, US |
| Decision | Substantially Equivalent, Sep 20, 1983 |
| Received | Jul 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832481
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.