American Medical Products, Inc. · Class II · Cleared Mar 17, 1983
| K-number | K823827 |
| Device name | AMP 80/2 OUTFLOW MONITOR MODIFICATION |
| Applicant | American Medical Products, Inc. |
| Product code | FKX |
| Device class | Class II |
| Decision date | Mar 17, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 876.5630 |
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