Triton Technology, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K932142 | SUCTION GUILLOTINE DEVICE | September 24, 1993 |
| K911448 | MULTIPLE BIOPSY DEVICE-MBX | April 16, 1991 |
| K902883 | TISSUE/POLYP TRAP SYSTEM | September 12, 1990 |
| K881303 | TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER | November 29, 1988 |