The following data is part of a premarket notification filed by Bisco, Inc. with the FDA for Biscem Translucent, Biscem Opaque.
Device ID | K060701 |
510k Number | K060701 |
Device Name: | BISCEM TRANSLUCENT, BISCEM OPAQUE |
Classification | Cement, Dental |
Applicant | BISCO, INC. 1100 WEST IRVING PARK RD. Schaumburg, IL 60193 |
Contact | Benjamin Lichtenwalner |
Correspondent | Benjamin Lichtenwalner BISCO, INC. 1100 WEST IRVING PARK RD. Schaumburg, IL 60193 |
Product Code | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-03-16 |
Decision Date | 2006-05-15 |
Summary: | summary |