K240227 is an FDA 510(k) clearance for the LiNA CystoVu? HD (CYV-100-5; CYV-101-5); LiNA ScopeVu? (SCP-100-1), a Cystoscope And Accessories, Flexible/rigid (Class II — Special Controls, product code FAJ), submitted by Lina Medical Aps (Glostrup, DK). The FDA issued a Cleared decision on August 22, 2024, 209 days after receiving the submission on January 26, 2024. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K240227 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 26, 2024 |
| Decision Date | August 22, 2024 |
| Days to Decision | 209 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | FAJ — Cystoscope And Accessories, Flexible/rigid |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | To Examine And Perform Procedures Within The Urinary Tract. For Reusable, Flexible Endoscopes In This Product Code, Validated Reprocessing Instructions And Reprocessing Validation Data Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf). |