VERSA LITE
Light, Ultraviolet, Dermatological
DIOMEDICS, INC.
The following data is part of a premarket notification filed by Diomedics, Inc. with the FDA for Versa Lite.
Pre-market Notification Details
| Device ID | K073503 |
| 510k Number | K073503 |
| Device Name: | VERSA LITE |
| Classification | Light, Ultraviolet, Dermatological |
| Applicant | DIOMEDICS, INC. 24372 MCCLOUD CT. Laguna Niguel, CA 92677 |
| Contact | Gary Mocnik |
| Correspondent | Gary Mocnik DIOMEDICS, INC. 24372 MCCLOUD CT. Laguna Niguel, CA 92677 |
| Product Code | FTC |
| CFR Regulation Number | 878.4630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-12-13 |
| Decision Date | 2008-01-23 |
Trademark Results [VERSA LITE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VERSA LITE 74293379 not registered Dead/Abandoned |
Pelican Products, Inc. 1992-07-13 |
 VERSA LITE 73588603 1485184 Dead/Cancelled |
VISTA MANUFACTURING, INC. 1986-03-17 |
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