510(k) K230133 ยท QFQ Ingested, Transient, Space Occupying Device For Weight Management And/Or Weight Loss
Plenity
| Applicant | Gelesis, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Jan 19, 2024 |
| Received | Jan 17, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230133
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.