Immunicon Corp. · Class I · Cleared Sep 30, 2002
| K-number | K022512 |
| Device name | CELLPREP SAMPLE PREPARATION SYSTEM, MODEL 9518 |
| Applicant | Immunicon Corp. |
| Product code | GKH |
| Device class | Class I |
| Decision date | Sep 30, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 864.5240 |
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