CooperSurgical, Inc. · Class II · Cleared Aug 6, 1997
| K-number | K971837 |
| Device name | VERRES NEEDLE, CANNULA FOR M820, CANNULA W/TRUMPET VALVE FOR M 820 |
| Applicant | CooperSurgical, Inc. |
| Product code | HET |
| Device class | Class II |
| Decision date | Aug 6, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 884.1720 |
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