The following data is part of a premarket notification filed by Sybron Dental Specialties, Inc. with the FDA for Belleglashp.
| Device ID | K955331 |
| 510k Number | K955331 |
| Device Name: | BELLEGLASHP |
| Classification | Crown And Bridge, Temporary, Resin |
| 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 | EBG |
| CFR Regulation Number | 872.3770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-11-20 |
| Decision Date | 1996-01-02 |