510(k) K851742 ยท KZF Device, Medical Examination, Ac Powered
MEDICAL EXAMINATION LIGHTS
| Applicant | Burton Medical Products Corp., Van Nuys CA, US |
| Decision | Substantially Equivalent, May 13, 1985 |
| Received | Apr 29, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851742
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 20, 2004 | Burton Medical Products Corp All Outpatient and Coolspot single ceiling or single track Medical Examination Lights manufactured before August 2000. Products manufactured during or after August 2000 contain a redesigned pivot asse Terminated |
KZF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.