Ron-Tech Medical , Ltd. · Class II · Cleared Aug 27, 1999
| K-number | K992071 |
| Device name | TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE |
| Applicant | Ron-Tech Medical , Ltd. |
| Product code | HDC |
| Device class | Class II |
| Decision date | Aug 27, 1999 |
| Decision | Substantially Equivalent |
| Regulation | 884.4530 |
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