510(k) K052241 ยท HRX Arthroscope
DISC-FX SYSTEM
| Applicant | Ellman International, Inc., Oceanside NY, US |
| Decision | Substantially Equivalent, Feb 24, 2006 |
| Received | Aug 17, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052241
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.