K191073 is an FDA 510(k) clearance for the Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter. This device is classified as a Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed (Class II - Special Controls, product code NUJ).
Submitted by Vein 360, LLC (Blue Ash, US). The FDA issued a Cleared decision on October 22, 2019, 183 days after receiving the submission on April 22, 2019.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4400. Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission. (70 Fr 56911, Available At Https://www.govinfo.gov/content/pkg/fr-2005-09-29/pdf/05-19510.pdf)..
| 510(k) Number | K191073 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 22, 2019 |
| Decision Date | October 22, 2019 |
| Days to Decision | 183 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | NUJ — Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4400 |
| Definition | Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission. (70 Fr 56911, Available At Https://www.govinfo.gov/content/pkg/fr-2005-09-29/pdf/05-19510.pdf). |