The following data is part of a premarket notification filed by Neomed, Inc. with the FDA for Neomed Enteral Feeding Tube.
| Device ID | K072881 |
| 510k Number | K072881 |
| Device Name: | NEOMED Enteral FEEDING TUBE |
| Classification | Tube, Feeding |
| Applicant | NEOMED, INC. 717 LAKEGLEN DR. Suwanee, GA 30024 |
| Contact | Penny Northcutt |
| Correspondent | Penny Northcutt NEOMED, INC. 717 LAKEGLEN DR. Suwanee, GA 30024 |
| Product Code | FPD |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-09 |
| Decision Date | 2008-01-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20350770002167 | K072881 | 000 |
| 20350770000811 | K072881 | 000 |
| 00350770000800 | K072881 | 000 |
| 00350770000794 | K072881 | 000 |
| 20350770000781 | K072881 | 000 |
| 20350770000774 | K072881 | 000 |
| 00350770000763 | K072881 | 000 |
| 00350770000756 | K072881 | 000 |
| 00350770000749 | K072881 | 000 |
| 20350770000736 | K072881 | 000 |
| 00350770000725 | K072881 | 000 |
| 20350770000712 | K072881 | 000 |
| 20350770000828 | K072881 | 000 |
| 00350770000831 | K072881 | 000 |
| 00350770000848 | K072881 | 000 |
| 00350770002156 | K072881 | 000 |
| 20350770002143 | K072881 | 000 |
| 00350770002132 | K072881 | 000 |
| 20350770002129 | K072881 | 000 |
| 20350770002112 | K072881 | 000 |
| 00350770002101 | K072881 | 000 |
| 00350770002095 | K072881 | 000 |
| 00350770002088 | K072881 | 000 |
| 20350770000873 | K072881 | 000 |
| 20350770000866 | K072881 | 000 |
| 00350770000855 | K072881 | 000 |
| 20350770000705 | K072881 | 000 |