Welch Allyn, Inc. · Class II · Cleared May 21, 1993
| K-number | K925899 |
| Device name | AMBULATORY BLOOD PRESSURE MONITOR, MDL# 5100-01 |
| Applicant | Welch Allyn, Inc. |
| Product code | DSK |
| Device class | Class II |
| Decision date | May 21, 1993 |
| Decision | Substantially Equivalent |
| Regulation | 870.1110 |
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