510(k) K191881 ยท LEJ Booth, Sun Tan
KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun
| Applicant | Kbl GmbH, Dernbach, DE |
| Decision | Substantially Equivalent, Oct 28, 2019 |
| Received | Jul 15, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191881
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.