The following data is part of a premarket notification filed by Ivoclar Usa, Inc. with the FDA for Sr 3/60 Nf Denture Mater. & Self-cure Dent. Resin.
Device ID | K864708 |
510k Number | K864708 |
Device Name: | SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN |
Classification | Resin, Denture, Relining, Repairing, Rebasing |
Applicant | IVOCLAR USA, INC. BAUER, CHENG & ASSOCIATES 111 N. WABASH Chicago, IL 60602 |
Contact | Bauer, Phd |
Correspondent | Bauer, Phd IVOCLAR USA, INC. BAUER, CHENG & ASSOCIATES 111 N. WABASH Chicago, IL 60602 |
Product Code | EBI |
CFR Regulation Number | 872.3760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-12-02 |
Decision Date | 1987-02-25 |