Intl. Hospital Products, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K841443 | REDO CENTRAL VENOUS CATHETER-NEONATE | LJS | 1984-07-27 | View |
| 510(k) | K792333 | BAKER INTESTINAL TUBE, TWIN CUFF | KNT | 1980-01-16 | View |
No matching devices.
Advertisement