The following data is part of a premarket notification filed by Heraeus Kulzer, Inc. with the FDA for Flow Line.
Device ID | K990756 |
510k Number | K990756 |
Device Name: | FLOW LINE |
Classification | Material, Tooth Shade, Resin |
Applicant | HERAEUS KULZER, INC. 4315 SOUTH LAFAYETTE BLVD. South Bend, IN 46614 -2517 |
Contact | Cheryl V Zimmerman |
Correspondent | Cheryl V Zimmerman HERAEUS KULZER, INC. 4315 SOUTH LAFAYETTE BLVD. South Bend, IN 46614 -2517 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-03-08 |
Decision Date | 1999-05-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLOW LINE 86491374 4953803 Live/Registered |
FLOWLINE VALVE AND CONTROLS, L.L.C. 2014-12-29 |
FLOW LINE 75594993 2484191 Live/Registered |
KULZER GMBH 1998-12-01 |