The following data is part of a premarket notification filed by Chayes Virginia, Inc. with the FDA for Dentiscope.
| Device ID | K820907 |
| 510k Number | K820907 |
| Device Name: | DENTISCOPE |
| Classification | Light, Fiber Optic, Dental |
| Applicant | CHAYES VIRGINIA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EAY |
| CFR Regulation Number | 872.4620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-04-01 |
| Decision Date | 1982-05-05 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DENTISCOPE 90168049 not registered Live/Pending |
DentiScope Corporation 2020-09-09 |
![]() DENTISCOPE 73360671 1244333 Dead/Cancelled |
Johnson & Johnson 1982-04-19 |