K180068 is an FDA 510(k) clearance for the ORISE Gel, a Submucosal Injection Agent (Class II — Special Controls, product code PLL), submitted by Boston Scientific (Marborough, US). The FDA issued a Cleared decision on September 28, 2018, 262 days after receiving the submission on January 9, 2018. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.
| 510(k) Number | K180068 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 09, 2018 |
| Decision Date | September 28, 2018 |
| Days to Decision | 262 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | PLL — Submucosal Injection Agent |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.1500 |
| Definition | Intended For Use In Gastrointestinal Endoscopic Procedures For Submucosal Lift Of Polyps, Adenomas, Early-stage Cancers Or Other Gastrointestinal Mucosal Lesions, Prior To Excision With A Snare Or Endoscopic Device. |