LIGHT-PAK
Light, Fiber Optic, Dental
MIDWEST
The following data is part of a premarket notification filed by Midwest with the FDA for Light-pak.
Pre-market Notification Details
| Device ID | K791733 |
| 510k Number | K791733 |
| Device Name: | LIGHT-PAK |
| Classification | Light, Fiber Optic, Dental |
| Applicant | MIDWEST 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 | 1979-08-28 |
| Decision Date | 1979-10-23 |
Trademark Results [LIGHT-PAK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LIGHT-PAK 73250084 1188532 Dead/Cancelled |
American Hospital Supply Corporation 1980-02-13 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.