K120935 is an FDA 510(k) clearance for the SECURACATH. This device is classified as a Implanted Subcutaneous Securement Catheter (Class II - Special Controls, product code OKC).
Submitted by Interrad Medical, Inc. (Minneapolis, US). The FDA issued a Cleared decision on April 27, 2012, 30 days after receiving the submission on March 28, 2012.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.5970. Access To Central Venous System For Blood Sampling And Infusion, And To Provide A Means To Secure The Catheter Via A Subcutaneous Anchor Below The Insertion Site..
| 510(k) Number | K120935 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 28, 2012 |
| Decision Date | April 27, 2012 |
| Days to Decision | 30 days |
| Submission Type | Special |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | OKC - Implanted Subcutaneous Securement Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 880.5970 |
| Definition | Access To Central Venous System For Blood Sampling And Infusion, And To Provide A Means To Secure The Catheter Via A Subcutaneous Anchor Below The Insertion Site. |