| K-number | K042414 |
| Device name | VISIOPLAST ACRYLIC RESIN |
| Applicant | Tecres |
| Product code | GXP |
| Device class | Class II |
| Decision date | Dec 29, 2004 |
| Decision | Substantially Equivalent |
| Regulation | 882.5300 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov