Erika, Inc. · Class II · Cleared Aug 30, 1982
| K-number | K822485 |
| Device name | HPF 100,200,300 CAPILLARY FLOW DIALYZ |
| Applicant | Erika, Inc. |
| Product code | FKQ |
| Device class | Class II |
| Decision date | Aug 30, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 876.5820 |
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