| K-number | K851052 |
| Device name | TUBULITEC PRIMER |
| Applicant | Dental Therapeutics AB |
| Product code | LBH |
| Device class | Class II |
| Decision date | Jul 31, 1985 |
| Decision | Substantially Equivalent |
| Regulation | 872.3260 |
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