The following data is part of a premarket notification filed by Hdc Corp. with the FDA for Enteral Feeding Tube.
| Device ID | K890116 |
| 510k Number | K890116 |
| Device Name: | ENTERAL FEEDING TUBE |
| Classification | Tube, Feeding |
| Applicant | HDC CORP. 2551 CASEY AVE. Mountain View, CA 94043 |
| Contact | L Coleman |
| Correspondent | L Coleman HDC CORP. 2551 CASEY AVE. Mountain View, CA 94043 |
| Product Code | FPD |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-11 |
| Decision Date | 1989-04-05 |