510(k) K180994 ยท KMK Device, Intravascular Catheter Securement
SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F
| Applicant | Interrad Medical, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jul 9, 2019 |
| Received | Apr 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180994
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.