Cutler Laboratories, 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) | K781785 | I.V. SET WITH IN-LINE FILTER | FPA | 1978-12-07 | View |
| 510(k) | K781140 | CUTTER RESIFLEX FOLEY CATHETERS | DJC | 1978-09-07 | View |
No matching devices.
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