510(k) K970642 ยท HRX Arthroscope
TENOSCOPE
| Applicant | Luxtec Corp., Newton MA, US |
| Decision | Substantially Equivalent, May 21, 1997 |
| Received | Feb 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970642
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.