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 |