The following data is part of a premarket notification filed by Parker Laboratories, Inc. with the FDA for Provit.
| Device ID | K800060 |
| 510k Number | K800060 |
| Device Name: | PROVIT |
| Classification | Cement, Dental |
| Applicant | PARKER LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EMA |
| CFR Regulation Number | 872.3275 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-01-10 |
| Decision Date | 1980-01-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PROVIT 87556819 not registered Dead/Abandoned |
IOSO LLC 2017-08-04 |
![]() PROVIT 78046070 not registered Dead/Abandoned |
Khan, Majid Abdul 2001-02-01 |
![]() PROVIT 73784342 1562001 Dead/Cancelled |
B&R INDUSTRIAL AUTOMATION CORPORATION 1989-03-03 |