510(k) K914784 ยท KQA Device, Beam Limiting, X-Ray, Therapeutic
PAPILLION PROCTOSCOPE
| Applicant | Oldelft Corp. of America, Fairfax VA, US |
| Decision | Substantially Equivalent, Jun 5, 1992 |
| Received | Oct 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914784
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.