510(k) K821909 ยท LDE Stethoscope, Manual
LITTMAN TUNABLE STETHOSCOPE 2136
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, Jul 14, 1982 |
| Received | Jun 28, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821909
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.