Dey Laboratories, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K972778 | DEY VIAL SODIUM CHLORIDE 3% | CAF | 1997-10-08 | View |
| 510(k) | K910239 | NEBU-SOL METERED DOSE DISPENSER (TM) | BSY | 1991-05-22 | View |
| 510(k) | K880411 | DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILE | CAF | 1988-02-29 | View |
| 510(k) | K875011 | DEY-PAK PURIFIED WATER, USP, STERILE | CCQ | 1988-01-22 | View |
| 510(k) | K875024 | DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP | CCQ | 1988-01-22 | View |
| 510(k) | K831532 | OCULAR IRRIGATING CANNULA | HMX | 1983-07-12 | View |
No matching devices.
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