510(k) K811911 ยท DXJ Display, Cathode-Ray Tube, Medical
SINGLE CHANNEL NON-FADE OSCILLOSCOPE
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 28, 1981 |
| Received | Jul 1, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811911
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.