Sumitomo Electric Industries, Inc. · Class II · Cleared Jul 27, 1981
| K-number | K811836 |
| Device name | PO-200 BLOOD OXYGEN MONITOR |
| Applicant | Sumitomo Electric Industries, Inc. |
| Product code | KLK |
| Device class | Class II |
| Decision date | Jul 27, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 868.2500 |
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