STERIS Corporation · Class II · Cleared Dec 13, 2001
| K-number | K013242 |
| Device name | AMSCO HARMONY SURGICAL LIGHTING AND MEDIA SYSTEM |
| Applicant | STERIS Corporation |
| Product code | FTD |
| Device class | Class II |
| Decision date | Dec 13, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 878.4580 |
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