The following data is part of a premarket notification filed by Medline Industries, Inc. with the FDA for Dynafeed.
| Device ID | K854215 |
| 510k Number | K854215 |
| Device Name: | DYNAFEED |
| Classification | Tubes, Gastrointestinal (and Accessories) |
| Applicant | MEDLINE INDUSTRIES, INC. ONE MEDLINE PLACE Mundelein, IL 60060 |
| Contact | Robert Fasana |
| Correspondent | Robert Fasana MEDLINE INDUSTRIES, INC. ONE MEDLINE PLACE Mundelein, IL 60060 |
| Product Code | KNT |
| CFR Regulation Number | 876.5980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-10-17 |
| Decision Date | 1985-12-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DYNAFEED 88430923 not registered Live/Pending |
6348017 CANADA Inc. 2019-05-15 |
![]() DYNAFEED 87265225 5552955 Live/Registered |
FAR EASTERN NEW CENTURY CORPORATION 2016-12-12 |