Globe Management Support, 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) | K960702 | CRP-LATEX SEIKEN XR REAGENT SYSTEM | DCK | 1996-04-19 | View |
| 510(k) | K960703 | RF-LATEX SEIKEN REAGENT SYSTEM | DHR | 1996-04-19 | View |
No matching devices.
Advertisement