I-Flow, LLC
I-Flow, LLC holds FDA 510(k) medical device clearance, cleared in 2014, with 2 FDA device recalls on record.
Top product codes for I-Flow, LLC
FDA recalls by I-Flow, LLC
- Z-1444-2013 — I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Tray, Model #TBTB1089T The intended use of each component in the finished final trays is consistent with the intended use of the component stated in the respective 510(k) submission.
- Z-1445-2013 — I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Kit, Model #TB089T The intended use of each component in the finished final trays is consistent with the intended use of the component stated in the respective 510(k) submission.
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 I-Flow, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.