Diagnostic Products Corp. · Class II · Cleared Feb 26, 1999
| K-number | K990222 |
| Device name | IMMULITE HCG, MODEL LKCG1, LCCG5, IMMULITE 2000 HCG, MODEL L2KCG2, L2KCG6 |
| Applicant | Diagnostic Products Corp. |
| Product code | DHA |
| Device class | Class II |
| Decision date | Feb 26, 1999 |
| Decision | Substantially Equivalent |
| Regulation | 862.1155 |
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