Cobe Laboratories, Inc. · Class II · Cleared Dec 10, 1980
| K-number | K802250 |
| Device name | DIALYSIS CONTROL UNIT-CENTRY 2000 |
| Applicant | Cobe Laboratories, Inc. |
| Product code | FKP |
| Device class | Class II |
| Decision date | Dec 10, 1980 |
| Decision | Substantially Equivalent |
| Regulation | 876.5820 |
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