FDA Product Code
FDA Product Code OKC — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General Hospital
- 21 CFR Citation
- 880.5970
510(k) Clearances — 5 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K210629 | SecurAcath | Interrad Medical, Inc. | 2021-04-12 | Special | PDF ↗ |
| K180769 | SecurAcath | Interrad Medical, Inc. | 2018-06-26 | Special | PDF ↗ |
| K120935 | SECURACATH | Interrad Medical, Inc. | 2012-04-27 | Special | PDF ↗ |
| K083081 | MODIFICATION TO SECURACATH, MODEL: SPK01 | Interrad Medical, Inc. | 2009-03-04 | Traditional | PDF ↗ |
| K082047 | SECURACATH CATHETER, MODEL SPK01 | Interrad Medical, Inc. | 2008-09-30 | Traditional | PDF ↗ |
Product code OKC · Class II · General Hospital. Data: openFDA.