510(k) K182196 ยท DQD Stethoscope, Electronic
Cardiart Electronic Stethoscope Model DS101 Omni-Steth Electronic Stethoscope Model Omni-Steth
| Applicant | Imediplus, Inc., Chupei City, TW |
| Decision | Substantially Equivalent, Sep 11, 2018 |
| Received | Aug 14, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182196
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.