510(k) K885161
K885161 is an FDA 510(k) premarket notification submitted by Voss Medical Products for the device "VOSS VEIN CLAMP". The FDA issued a decision of Substantially Equivalent on December 22, 1989. The device falls under product code DXC (Clamp, Vascular), a Class II device regulated under 21 CFR 870.4450. Voss Medical Products has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 22, 1989
- Date Received
- December 13, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Clamp, Vascular
- Device Class
- Class II
- Regulation Number
- 870.4450
- Review Panel
- CV
- Submission Type