The following data is part of a premarket notification filed by Corpak Medsystems with the FDA for Neonatal Nasogastric Feeding Tube-.
| Device ID | K831328 |
| 510k Number | K831328 |
| Device Name: | NEONATAL NASOGASTRIC FEEDING TUBE- |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | CORPAK MEDSYSTEMS 1001 Asbury Dr Buffalo Grove, IL 60089 |
| Contact | Stephanie Wasielewski |
| Correspondent | Stephanie Wasielewski CORPAK MEDSYSTEMS 1001 Asbury Dr Buffalo Grove, IL 60089 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-04-25 |
| Decision Date | 1983-07-19 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10350770460755 | K831328 | 000 |
| 10350770457670 | K831328 | 000 |
| 10350770457694 | K831328 | 000 |
| 10350770460359 | K831328 | 000 |
| 10350770460366 | K831328 | 000 |
| 10350770460373 | K831328 | 000 |
| 10350770460700 | K831328 | 000 |
| 10350770460717 | K831328 | 000 |
| 10350770460724 | K831328 | 000 |
| 10350770460731 | K831328 | 000 |
| 10350770460748 | K831328 | 000 |
| 10350770457649 | K831328 | 000 |