Andon Health Co, Ltd. · Class II · Cleared Feb 27, 2009
| K-number | K083395 |
| Device name | SEMI-FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODELS: KD-322,KD-622,KD-575,KD-525E,KD-593,KD-595,KD-596,KD-598 |
| Applicant | Andon Health Co, Ltd. |
| Product code | DXN |
| Device class | Class II |
| Decision date | Feb 27, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 870.1130 |
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