Velocimed
Velocimed appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 7, 2006.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K052523 | PROXIS SYSTEM | September 7, 2006 |
| K043084 | PREMERE DELIVERY SHEATH, MODEL PDS | May 2, 2005 |
| K042117 | PROXIS SYSTEM, MODEL EPS 101 | January 7, 2005 |
| K042910 | VENTURE WIRE CONTROL CATHETER, MODEL WCC | November 22, 2004 |
| K040922 | VENTURE WIRE CONTROL CATHETER | August 18, 2004 |
| K023548 | PROXIS FLOW-CONTROL DEVICE, MODELS EPS 101, IC 101 | August 4, 2003 |