510(k) K082194 ยท HRX Arthroscope
LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002
| Applicant | Laurimed, LLC, Redwood City CA, US |
| Decision | Substantially Equivalent, Aug 28, 2008 |
| Received | Aug 4, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082194
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.