Quinton, Inc. · Class II · Cleared Dec 29, 1987
| K-number | K874632 |
| Device name | BENT NECK CURLCATH PERITONEAL DIALYSIS KIT |
| Applicant | Quinton, Inc. |
| Product code | FKX |
| Device class | Class II |
| Decision date | Dec 29, 1987 |
| 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