Company ยท US
Velocimed, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2006. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 7, 2006 | K052523 | PROXIS SYSTEM Velocimed, Inc. | NFA |
| May 2, 2005 | K043084 | PREMERE DELIVERY SHEATH, MODEL PDS Velocimed, Inc. | DYB |
| Jan 7, 2005 | K042117 | PROXIS SYSTEM, MODEL EPS 101 Velocimed, Inc. | DQY |
| Nov 22, 2004 | K042910 | VENTURE WIRE CONTROL CATHETER, MODEL WCC Velocimed, Inc. | DQY |
| Aug 18, 2004 | K040922 | VENTURE WIRE CONTROL CATHETER Velocimed, Inc. | DQY |
| Aug 4, 2003 | K023548 | PROXIS FLOW-CONTROL DEVICE, MODELS EPS 101, IC 101 Velocimed | DQY |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||