Enteral Feeding Container
FDA 510(k) K890424 · Multi-Med, Inc.
510(k) numberK890424
Submission
- Device name
- Enteral Feeding Container
- Applicant
- Multi-Med, Inc.
West Swanzey, NH, US - Received
- January 26, 1989
- Decision date
- June 14, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KNT – Tubes, Gastrointestinal (And Accessories)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5980
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code KNT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261890 | 52Fr ViSiGi LUX; 52Fr ViSiGi 3D®KNT · Special | Boehringer Laboratories, LLC | 08/14/2026SE |
| K253514 | Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore…KNT · Traditional | C.R. Bard, Inc. | 07/10/2026SE |
| K250389 | XNY Disposable Gastric Calibration TubeKNT · Traditional | Changzhou Xin Neng Yuan Medical Stapler Co.,Ltd | 04/10/2025SE |
| K243228 | Flexi-Seal AIR (with ENFit Connector)KNT · Traditional | Convatec | 03/28/2025SE |
| K242336 | hygh-tec Drainage IIKNT · Traditional | Amb Medtec | 01/17/2025SE |
| K242901 | ZZIREN Orogastric Tube; ZZIREN SGT Orogastric Tube - 32 Fr (ZZ-SGT-32); ZZIREN SGT…KNT · Traditional | Tools For Surgery, LLC | 01/10/2025SE |
| K241169 | Entarik NI Feeding Tube SystemKNT · Traditional | Gravitas Medical, Inc. | 11/22/2024SE |
| K241185 | CORGRIP* SR NG/NI Tube Retention SystemKNT · Traditional | Avanos Medical, Inc. | 10/25/2024SE |
| K240965 | CORTRAK* 2 Enteral Access System (20-0950)KNT · Traditional | Avanos Medical, Inc. | 06/06/2024SE |
| K233591 | StylusKNT · Traditional | Degania Silicone , Ltd. | 05/31/2024SE |
More from Degania Silicone , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K120195 | Safety Subcutaneous Tissue Infusion SetFPA · Traditional | 07/06/2012SE |
| K890396 | External Feeding Set for Pump UseFPD · Traditional | 05/23/1989SE |
| K891176 | Injection Site Plug (Intravascular Administration)FPA · Traditional | 05/18/1989SE |
| K891919 | Intravascular Administration SetFMI · Traditional | 05/05/1989SE |
| K891072 | Intravascular Administration SetFPA · Traditional | 04/21/1989SE |
| K890340 | Intravascular Administration SetFPA · Traditional | 03/31/1989SE |
| K890127 | Intravascular Administration SetFMI · Traditional | 02/03/1989SE |
Questions and answers
When was Enteral Feeding Container cleared by the FDA?
Enteral Feeding Container (K890424) received a 510(k) decision of Substantially Equivalent on June 14, 1989, 139 days after the submission was received.
What is the product code of K890424?
The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.