510(k) K973162 ยท IWE Monitor, Patient Position, Light-Beam
DUAL RADIATION TARGETING SYSTEM DRTS DRAPE
| Applicant | Hogan & Hartson, Washington DC, US |
| Decision | Substantially Equivalent, Nov 20, 1997 |
| Received | Aug 22, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973162
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.