510(k) K954476 ยท HRX Arthroscope
PROBE
| Applicant | Phx Technologies Corp., Denton TX, US |
| Decision | Substantially Equivalent, Oct 23, 1995 |
| Received | Sep 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954476
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.