The following data is part of a premarket notification filed by Medlogic Global Corp. with the FDA for Liquiband Dental.
| Device ID | K993556 |
| 510k Number | K993556 |
| Device Name: | LIQUIBAND DENTAL |
| Classification | Cement, Dental |
| Applicant | MEDLOGIC GLOBAL CORP. 4815 LIST DR., SUITE 111 Colorado Springs, CO 80919 |
| Contact | Stephen J Tamsett |
| Correspondent | Stephen J Tamsett MEDLOGIC GLOBAL CORP. 4815 LIST DR., SUITE 111 Colorado Springs, CO 80919 |
| Product Code | EMA |
| CFR Regulation Number | 872.3275 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-10-20 |
| Decision Date | 2000-01-03 |
| Summary: | summary |