510(k) K800230 ยท KZF Device, Medical Examination, Ac Powered
ABCO EXAMINATION LAMP (GOOSENECK TYPE)
| Applicant | Abco Dealers, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 26, 1980 |
| Received | Feb 5, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800230
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.