The following data is part of a premarket notification filed by Bisco, Inc. with the FDA for Bisco Universal Bond-3.
Device ID | K923842 |
510k Number | K923842 |
Device Name: | BISCO UNIVERSAL BOND-3 |
Classification | Agent, Tooth Bonding, Resin |
Applicant | BISCO, INC. 1500 W. THORNDALE AVE. Itasca, IL 60143 |
Contact | Byoung I Suh |
Correspondent | Byoung I Suh BISCO, INC. 1500 W. THORNDALE AVE. Itasca, IL 60143 |
Product Code | KLE |
CFR Regulation Number | 872.3200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-31 |
Decision Date | 1992-09-29 |