Vasonova, Inc.
Vasonova, Inc. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2013, with 1 FDA device recall on record.
Top product codes for Vasonova, Inc.
FDA recalls by Vasonova, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Vasonova, Inc.
- K123813 — VASCULAR POSITIONING SYSTEM (VPS) G4 CONSOLE
- K103255 — VASCULAR POSITIONING SYSTEM TM (VPS TM SYSTEM) STYLET
- K103260 — VASCULAR POSITIONING SYSTEM (VPS SYSTEM) CONSOLE
- K091924 — VPS CATHETER
- K083920 — FLOWPICC CATHETER
- K082481 — FLOWPICC CATHETER
- K081626 — FLOWPICC CONSOLE
- K081625 — FLOWPICC STYLET
Data sourced from openFDA. This site is unofficial and independent of the FDA.