510(k) K913763
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 20, 1991
- Date Received
- August 22, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Angioscope
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- CV
- Submission Type