Mitsubishi Cable America, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K955717 | ENDOSCOPE INTRODUCER KIT | April 18, 1996 |
| K960081 | BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE | March 12, 1996 |
| K936257 | ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3 | March 24, 1994 |