Diagnostic Products Corp. · Class II · Cleared Dec 19, 1994
| K-number | K940006 |
| Device name | IMMULITE THIRD GENERATION (MODIFICATION) |
| Applicant | Diagnostic Products Corp. |
| Product code | JLW |
| Device class | Class II |
| Decision date | Dec 19, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 862.1690 |
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