Dey Laboratories, Inc.
Dey Laboratories, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 8, 1997.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K972778 | DEY VIAL SODIUM CHLORIDE 3% | October 8, 1997 |
| K910239 | NEBU-SOL METERED DOSE DISPENSER (TM) | May 22, 1991 |
| K880411 | DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILE | February 29, 1988 |
| K875011 | DEY-PAK PURIFIED WATER, USP, STERILE | January 22, 1988 |
| K875024 | DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP | January 22, 1988 |
| K831532 | OCULAR IRRIGATING CANNULA | July 12, 1983 |