| K-number | K961992 |
| Device name | NEEDLE'S EYE SNARE |
| Applicant | Cook Pacemaker Corp. |
| Product code | DXE |
| Device class | Class II |
| Decision date | Dec 27, 1996 |
| Decision | Substantially Equivalent |
| Regulation | 870.5150 |
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