American Omni Medical, Inc. · Class II · Cleared Oct 30, 1986
| K-number | K862950 |
| Device name | WHITE-SIPOSS TUBE, CAT NO WS-1 |
| Applicant | American Omni Medical, Inc. |
| Product code | BTR |
| Device class | Class II |
| Decision date | Oct 30, 1986 |
| Decision | Substantially Equivalent |
| Regulation | 868.5730 |
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