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 |