510(k) K945082 ยท LDE Stethoscope, Manual
CYPRESS MEDICAL PRODUCTS STETHOSCOPE
| Applicant | Cypress Medical Products, Ltd., Mc Henry IL, US |
| Decision | Substantially Equivalent, Dec 8, 1994 |
| Received | Oct 17, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945082
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.