510(k) K943802 ยท IWE Monitor, Patient Position, Light-Beam
HP BACK POINTER SYSTEM
| Applicant | Medtec, Inc., Orange City IA, US |
| Decision | Substantially Equivalent, Dec 7, 1994 |
| Received | Aug 4, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943802
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.