Amicon, Inc. · Class II · Cleared Jan 17, 1983
| K-number | K823881 |
| Device name | ARTERIOVENOUS BLOOD TUBING SET FOR |
| Applicant | Amicon, Inc. |
| Product code | KDI |
| Device class | Class II |
| Decision date | Jan 17, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 876.5860 |
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