The following data is part of a premarket notification filed by Pro Care Laboratories, Inc. with the FDA for Brushrite.
Device ID | K880442 |
510k Number | K880442 |
Device Name: | BRUSHRITE |
Classification | Analyzer, Gas, Argon, Gaseous-phase |
Applicant | PRO CARE LABORATORIES, INC. 218 WEST PARK ST. West Point, NE 68788 |
Contact | Eugene M Mueller |
Correspondent | Eugene M Mueller PRO CARE LABORATORIES, INC. 218 WEST PARK ST. West Point, NE 68788 |
Product Code | JEG |
CFR Regulation Number | 868.1075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-02-02 |
Decision Date | 1988-05-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BRUSHRITE 98762753 not registered Live/Pending |
Future Wave Products, Inc. 2024-09-21 |
BRUSHRITE 87601090 not registered Dead/Abandoned |
David G. Capper 2017-09-08 |
BRUSHRITE 74272254 not registered Dead/Abandoned |
Securus, Inc. 1992-05-04 |