Koven and Assoc., Inc. · Class II · Cleared Jan 22, 1993
| K-number | K920333 |
| Device name | SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTOR |
| Applicant | Koven and Assoc., Inc. |
| Product code | DPW |
| Device class | Class II |
| Decision date | Jan 22, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 870.2100 |
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