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Companies / The Kendall Company Div. of Tyco Healthcare Group
The Kendall Company Div. of Tyco Healthcare Group
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K024010 | DOVER SILVER HYDROGEL COATED SILICONE FOLEY CATHETER | June 11, 2003 |
| K831081 | EZEE FILTER/SEPARATOR | May 16, 1983 |
| K831082 | CONNECTING TUBING | May 9, 1983 |
| K831079 | LIQUIPETTE | April 28, 1983 |