The following data is part of a premarket notification filed by D-w Intl. with the FDA for Cedeta.
Device ID | K915717 |
510k Number | K915717 |
Device Name: | CEDETA |
Classification | Device, Electrical Dental Anesthesia |
Applicant | D-W INTL. 3212 SE 147TH PLACE SUITE 103 Vancouver, WA 98684 |
Contact | Charles R Whitlock |
Correspondent | Charles R Whitlock D-W INTL. 3212 SE 147TH PLACE SUITE 103 Vancouver, WA 98684 |
Product Code | LWM |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-12-19 |
Decision Date | 1992-11-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CEDETA 74361855 1804301 Dead/Cancelled |
Cedeta Research Limited 1993-02-22 |