Tsi, Inc. · Class II · Cleared Sep 19, 1988
| K-number | K875179 |
| Device name | MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403A |
| Applicant | Tsi, Inc. |
| Product code | DPW |
| Device class | Class II |
| Decision date | Sep 19, 1988 |
| 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