510(k) K151604 ยท MPA Endoilluminator
23ga Chandelier Illuminator, 25ga Chandelier Illuminator
| Applicant | Peregrine Surgical , Ltd., New Britain PA, US |
| Decision | Substantially Equivalent, Sep 11, 2015 |
| Received | Jun 15, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151604
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.