The following data is part of a premarket notification filed by Voco Gmbh with the FDA for Polibond.
Device ID | K924181 |
510k Number | K924181 |
Device Name: | POLIBOND |
Classification | Agent, Tooth Bonding, Resin |
Applicant | VOCO GMBH C/ONDA RESOURCES 790 WASHINGTON STREET, STE 301 Denver, CO 80203 |
Contact | Gail E Gillenwater |
Correspondent | Gail E Gillenwater VOCO GMBH C/ONDA RESOURCES 790 WASHINGTON STREET, STE 301 Denver, CO 80203 |
Product Code | KLE |
CFR Regulation Number | 872.3200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-08-19 |
Decision Date | 1992-10-16 |