Columbus Instruments Intl. Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K895791 | OXYMAX | March 28, 1990 |
| K861543 | CARDIOMAX-II | March 10, 1987 |
| K861100 | ISO-THERMEX | May 12, 1986 |
| K782036 | TREMOR MONITOR | January 23, 1979 |
| K771718 | CARDIOTHERM-500X | September 28, 1977 |