K243652 is an FDA 510(k) clearance for the Monoject? Enteral Syringe with ENFit Connector (401SE); Monoject? Enteral Syringe with ENFit Connector (403SE); Monoject? Enteral Syringe with ENFit Connector (406SE); Monoject? Enteral Syringe with ENFit Connector (412SE); Monoject? Enteral Syringe with ENFit Connector (435SE); Monoject? Enteral Syringe with ENFit Connector (460SE), a Enteral Syringes With Enteral Specific Connectors (Class II — Special Controls, product code PNR), submitted by Cardinalhealth (Waukegan, US). The FDA issued a Cleared decision on December 19, 2024, 23 days after receiving the submission on November 26, 2024. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5980.
| 510(k) Number | K243652 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 26, 2024 |
| Decision Date | December 19, 2024 |
| Days to Decision | 23 days |
| Submission Type | Special |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Statement |
| Product Code | PNR — Enteral Syringes With Enteral Specific Connectors |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.5980 |
| Definition | Delivers Nutrition, Medication, Or Hydration Orally Or To A Gastrointestinal Tube Or Extension Set Using Aami/cn3(ps):2014 Compliant Connectors. |