RESIL
Resin, Denture, Relining, Repairing, Rebasing
PARKER LABORATORIES, INC.
The following data is part of a premarket notification filed by Parker Laboratories, Inc. with the FDA for Resil.
Pre-market Notification Details
| Device ID | K840548 |
| 510k Number | K840548 |
| Device Name: | RESIL |
| Classification | Resin, Denture, Relining, Repairing, Rebasing |
| Applicant | PARKER LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EBI |
| CFR Regulation Number | 872.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-08 |
| Decision Date | 1984-04-17 |
Trademark Results [RESIL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RESIL 98066364 not registered Live/Pending |
Osvaldo Torrez 2023-06-30 |
 RESIL 73160631 1123960 Dead/Cancelled |
RESIL S/A 1978-03-02 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.