Pie Medical Equipment B.V. · Class II · Cleared Oct 9, 1991
| K-number | K911043 |
| Device name | HEMISPHERE MULTIPLANE ENDORECTAL PROBE |
| Applicant | Pie Medical Equipment B.V. |
| Product code | ITX |
| Device class | Class II |
| Decision date | Oct 9, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 892.1570 |
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