The following data is part of a premarket notification filed by Sybron Dental Specialties, Inc. with the FDA for Sybraloy.
Device ID | K940675 |
510k Number | K940675 |
Device Name: | SYBRALOY |
Classification | Alloy, Amalgam |
Applicant | SYBRON DENTAL SPECIALTIES, INC. 1332 SOUTH LONE HILL AVE. Glendora, CA 91740 |
Contact | Jeffrey A Anderson |
Correspondent | Jeffrey A Anderson SYBRON DENTAL SPECIALTIES, INC. 1332 SOUTH LONE HILL AVE. Glendora, CA 91740 |
Product Code | EJJ |
CFR Regulation Number | 872.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-02-16 |
Decision Date | 1994-04-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SYBRALOY 73111386 1070881 Live/Registered |
SYBRON CORPORATION 1977-01-03 |