W.R. Grace & Co.-Conn.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K873887 | MODIFIED HOLLOW FIBERS USED IN DIAFILTER HEMOFIL. | KDI | 1987-12-09 | View |
| 510(k) | K860804 | MEDICAL ADHESIVE TAPE | KGX | 1986-03-24 | View |
No matching devices.
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