The following data is part of a premarket notification filed by Ivoclar North America, Inc. with the FDA for Targis System.
Device ID | K962878 |
510k Number | K962878 |
Device Name: | TARGIS SYSTEM |
Classification | Material, Tooth Shade, Resin |
Applicant | IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
Contact | Peter P Mancuso |
Correspondent | Peter P Mancuso IVOCLAR NORTH AMERICA, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-07-24 |
Decision Date | 1996-09-25 |