American Medical Devices, Inc. · Class I · Cleared May 20, 1997
| K-number | K970873 |
| Device name | ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.) |
| Applicant | American Medical Devices, Inc. |
| Product code | HMX |
| Device class | Class I |
| Decision date | May 20, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 886.4350 |
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