510(k) K181352 ยท DQA Oximeter
Loop System
| Applicant | Spry Health, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Mar 29, 2019 |
| Received | May 22, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181352
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.