510(k) DEN230041 ยท QZW Over-The-Counter Device To Assess Risk Of Sleep Apnea
Sleep Apnea Feature
| Applicant | Samsung Electronics Co., Ltd., Suwon-Si, KR |
| Decision | Unknown, Feb 6, 2024 |
| Received | May 31, 2023 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN230041
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.