The following data is part of a premarket notification filed by Southern Dental Industries, Inc. with the FDA for Galloy.
Device ID | K955285 |
510k Number | K955285 |
Device Name: | GALLOY |
Classification | Alloy, Amalgam |
Applicant | SOUTHERN DENTAL INDUSTRIES, INC. 246 FIRST ST., SUITE 204 San Francisco, CA 94105 |
Contact | Samantha Cheetham |
Correspondent | Samantha Cheetham SOUTHERN DENTAL INDUSTRIES, INC. 246 FIRST ST., SUITE 204 San Francisco, CA 94105 |
Product Code | EJJ |
CFR Regulation Number | 872.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-11-17 |
Decision Date | 1996-01-24 |