510(k) K946043 ยท ERA Otoscope
H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG
| Applicant | Rudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE |
| Decision | Unknown, Mar 8, 1995 |
| Received | Dec 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946043
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.