510(k) K945507 ยท KZF Device, Medical Examination, Ac Powered
H 5100, H 5200, H 5300
| Applicant | Rudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE |
| Decision | Substantially Equivalent, Dec 9, 1994 |
| Received | Nov 9, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945507
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.