FDA 510(k) Applications for Medical Device Product Code "OKC"
(Implanted Subcutaneous Securement Catheter)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K180769 | Interrad Medical Inc | SecurAcath | 06/26/2018 |
| K210629 | Interrad Medical Inc | SecurAcath | 04/12/2021 |
| K120935 | INTERRAD MEDICAL INC | SECURACATH | 04/27/2012 |
| K083081 | INTERRAD MEDICAL, INC. | MODIFICATION TO SECURACATH, MODEL: SPK01 | 03/04/2009 |
| K082047 | INTERRAD MEDICAL, INC. | SECURACATH CATHETER, MODEL SPK01 | 09/30/2008 |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact
