510(k) K190267
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 30, 2019
- Date Received
- February 8, 2019
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Valvulotome
- Device Class
- Class II
- Regulation Number
- 870.4885
- Review Panel
- CV
- Submission Type