510(k) K011974 ยท DQA Oximeter
SENSAID
| Applicant | Sensidyne, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Feb 12, 2002 |
| Received | Jun 25, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011974
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.