The following data is part of a premarket notification filed by Kerr Dental Materials Center with the FDA for Optibond Solo Plus 3.
Device ID | K011908 |
510k Number | K011908 |
Device Name: | OPTIBOND SOLO PLUS 3 |
Classification | Sealant, Pit And Fissure, And Conditioner |
Applicant | KERR DENTAL MATERIALS CENTER 1717 WEST COLLINS AVE. Orange, CA 92867 |
Contact | Colleen Boswell |
Correspondent | Colleen Boswell KERR DENTAL MATERIALS CENTER 1717 WEST COLLINS AVE. Orange, CA 92867 |
Product Code | EBC |
CFR Regulation Number | 872.3765 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-06-19 |
Decision Date | 2001-09-06 |
Summary: | summary |