510(k) DEN200028 ยท QIU Intense Pulsed Light Device For Managing Dry Eye
Lumenis Stellar M22
| Applicant | Lumenis, Ltd., Yokneam, IL |
| Decision | Unknown, Feb 23, 2021 |
| Received | Apr 20, 2020 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN200028
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.