Promedical , Ltd. · Class II · Cleared Oct 7, 1995
| K-number | K954596 |
| Device name | PRO-B CORE-RECT COAXIAL BIOPSY SYSTEM |
| Applicant | Promedical , Ltd. |
| Product code | FCG |
| Device class | Class II |
| Decision date | Oct 7, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 876.1075 |
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