EXTRUDE
Material, Impression
SYBRON DENTAL SPECIALTIES, INC.
The following data is part of a premarket notification filed by Sybron Dental Specialties, Inc. with the FDA for Extrude.
Pre-market Notification Details
| Device ID | K940379 |
| 510k Number | K940379 |
| Device Name: | EXTRUDE |
| Classification | Material, Impression |
| Applicant | SYBRON DENTAL SPECIALTIES, INC. 1332 SOUTH LONE HILL AVE. Glendora, CA 91740 |
| Contact | Larry Wills |
| Correspondent | Larry Wills SYBRON DENTAL SPECIALTIES, INC. 1332 SOUTH LONE HILL AVE. Glendora, CA 91740 |
| Product Code | ELW |
| CFR Regulation Number | 872.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-01-26 |
| Decision Date | 1994-03-22 |
Trademark Results [EXTRUDE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EXTRUDE 74023171 1621993 Dead/Cancelled |
Kerr Manufacturing Company 1990-01-29 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.