The following data is part of a premarket notification filed by Gc America, Inc. with the FDA for Fuji Ortho Lc.
| Device ID | K950556 |
| 510k Number | K950556 |
| Device Name: | FUJI ORTHO LC |
| Classification | Adhesive, Bracket And Tooth Conditioner, Resin |
| Applicant | GC AMERICA, INC. 3737 WEST 127TH ST. Alsip, IL 60803 |
| Contact | Terry L Joritz |
| Correspondent | Terry L Joritz GC AMERICA, INC. 3737 WEST 127TH ST. Alsip, IL 60803 |
| Product Code | DYH |
| CFR Regulation Number | 872.3750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-07 |
| Decision Date | 1995-03-08 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| D8281330121 | K950556 | 000 |