510(k) K191659 ยท FMF Syringe, Piston
Instylla Delivery Kit
| Applicant | Instylla, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Oct 10, 2019 |
| Received | Jun 21, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191659
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.