Hemocue, Inc. · Class II · Cleared Jun 10, 2004
| K-number | K041234 |
| Device name | HEMOCUE HEMOGLOBIN 201DM ANALYZING SYSTEM |
| Applicant | Hemocue, Inc. |
| Product code | GKR |
| Device class | Class II |
| Decision date | Jun 10, 2004 |
| Decision | Substantially Equivalent |
| Regulation | 864.5620 |
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