510(k) K800140 ยท HQX Implant, Orbital, Extra-Ocular
SILASTIC SCLERAL SPONGE II W/CIRCLING BD
| Applicant | Dow Corning Corp. Healthcare Industries Materials, Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 3, 1980 |
| Received | Jan 21, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800140
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.