The following data is part of a premarket notification filed by Heraeus Kulzer, Inc. with the FDA for Pre-vision Fill.
Device ID | K993602 |
510k Number | K993602 |
Device Name: | PRE-VISION FILL |
Classification | Material, Tooth Shade, Resin |
Applicant | HERAEUS KULZER, INC. 4315 SOUTH LAFAYETTE BLVD. South Bend, IN 46614 -2517 |
Contact | Cheryl V Zimmerman |
Correspondent | Cheryl V Zimmerman HERAEUS KULZER, INC. 4315 SOUTH LAFAYETTE BLVD. South Bend, IN 46614 -2517 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-10-25 |
Decision Date | 1999-12-15 |