510(k) K912128 ยท LDE Stethoscope, Manual
MAXI-SCOPE OR ULTRA-SCOPE
| Applicant | Seiichi Mfg., Inc., Jamestown KY, US |
| Decision | Substantially Equivalent, Jun 28, 1991 |
| Received | May 14, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912128
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.