K143344 is an FDA 510(k) clearance for the NeoMed NeoConnect Enteral Syringes with ENFit Connector, a Enteral Syringes With Enteral Specific Connectors (Class II — Special Controls, product code PNR), submitted by Neomed, Inc. (Woodstock, US). The FDA issued a Cleared decision on April 9, 2015, 139 days after receiving the submission on November 21, 2014. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5980.
| 510(k) Number | K143344 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 21, 2014 |
| Decision Date | April 09, 2015 |
| Days to Decision | 139 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| 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. |