The following data is part of a premarket notification filed by Gc America, Inc. with the FDA for Pattern Resin.
| Device ID | K003817 |
| 510k Number | K003817 |
| Device Name: | PATTERN RESIN |
| Classification | Crown And Bridge, Temporary, 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 | EBG |
| CFR Regulation Number | 872.3770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-12-11 |
| Decision Date | 2001-01-16 |