Cabot Medical Corp. · Class II · Cleared Jul 11, 1995
| K-number | K951714 |
| Device name | CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBER |
| Applicant | Cabot Medical Corp. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Jul 11, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
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