| K-number | K880021 |
| Device name | COBE CML3 |
| Applicant | Cobe Laboratories, Inc. |
| Product code | DTZ |
| Device class | Class II |
| Decision date | Apr 1, 1988 |
| Decision | Substantially Equivalent |
| Regulation | 870.4350 |
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