Med-Lectric Corporation · Class II · Cleared Dec 7, 2007
| K-number | K071878 |
| Device name | DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB |
| Applicant | Med-Lectric Corporation |
| Product code | GZJ |
| Device class | Class II |
| Decision date | Dec 7, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 882.5890 |
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