The following data is part of a premarket notification filed by Essential Dental Systems, Inc. with the FDA for Ti-core New & Improved.
Device ID | K922252 |
510k Number | K922252 |
Device Name: | TI-CORE NEW & IMPROVED |
Classification | Material, Tooth Shade, Resin |
Applicant | ESSENTIAL DENTAL SYSTEMS, INC. 55 NORTHERN BLVD. SUITE 301 Great Neck, NY 11021 |
Contact | Anand Akerkar |
Correspondent | Anand Akerkar ESSENTIAL DENTAL SYSTEMS, INC. 55 NORTHERN BLVD. SUITE 301 Great Neck, NY 11021 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-06 |
Decision Date | 1994-01-26 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00766054000211 | K922252 | 000 |
00766054000013 | K922252 | 000 |
00766054000006 | K922252 | 000 |