Great Eastern Lumber Co., Inc.
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) | K780708 | AUTOMATIC RETRACTOR HOLDER | GAD | 1978-07-17 | View |
| 510(k) | K780999 | X-RAY FRAME HOLDER | IZL | 1978-06-27 | View |
No matching devices.
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