| K-number | K871749 |
| Device name | ADULT PERM-CATH 40CM. |
| Applicant | Quinton, Inc. |
| Product code | LFJ |
| Device class | Class II |
| Decision date | Jun 17, 1987 |
| Decision | Substantially Equivalent |
| Regulation | 876.5540 |
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