Conmed Corporation · Class II · Cleared Oct 21, 2005
| K-number | K052104 |
| Device name | ULTRACLEAN HANDCONTROLLED SUCTION COAGULATOR, MODEL 130182, 130183, 130184, 130185; ULTRACLEAN FOOTCONTROLLED SUCTION |
| Applicant | Conmed Corporation |
| Product code | GEI |
| Device class | Class II |
| Decision date | Oct 21, 2005 |
| Decision | Substantially Equivalent |
| Regulation | 878.4400 |
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