510(k) K823792 ยท KOH Instrument, Manual, General Obstetric-Gynecologic
QUARTZ RETRACTOR/PROBE
| Applicant | American V. Mueller, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 18, 1983 |
| Received | Dec 15, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823792
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.