The following data is part of a premarket notification filed by Erich Jaeger, Inc. with the FDA for Flowscreen.
Device ID | K932744 |
510k Number | K932744 |
Device Name: | FLOWSCREEN |
Classification | Calculator, Predicted Values, Pulmonary Function |
Applicant | ERICH JAEGER, INC. P.O. BOX 10008 Rockford, IL 61131 |
Contact | Eichler |
Correspondent | Eichler ERICH JAEGER, INC. P.O. BOX 10008 Rockford, IL 61131 |
Product Code | BTY |
CFR Regulation Number | 868.1890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-08 |
Decision Date | 1994-03-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLOWSCREEN 79116161 4374104 Live/Registered |
eResearchTechnology GmbH 2012-07-09 |
FLOWSCREEN 78284719 not registered Dead/Abandoned |
Higginbotham, Edward Alan 2003-08-07 |
FLOWSCREEN 77243409 3487424 Live/Registered |
Technifex Products, LLC 2007-07-31 |
FLOWSCREEN 76364487 not registered Dead/Abandoned |
Technifex, Inc. 2002-01-29 |