Amsino International, Inc. · Class II · Cleared Oct 29, 2003
| K-number | K030120 |
| Device name | AMSURE FOLEY CATHETER |
| Applicant | Amsino International, Inc. |
| Product code | EZL |
| Device class | Class II |
| Decision date | Oct 29, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 876.5130 |
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