510(k) K213632 ยท FMF Syringe, Piston
Instylla Delivery Kit
| Applicant | Instylla, Inc., Bedford MA, US |
| Decision | Substantially Equivalent, Feb 10, 2022 |
| Received | Nov 17, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213632
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.