Thornhill Research, Inc.
Thornhill Research, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2019, with 2 FDA device recalls on record.
Top product codes for Thornhill Research, Inc.
FDA recalls by Thornhill Research, Inc.
- Z-0586-2016 — MOVES System, an emergency ventilator with suction, oxygen concentrator and multi-parameter patient monitoring capabilities. The MOVES System is a portable computer controlled electrically powered transport emergency ventilator intended to provide continuous or intermittent ventilatory support for the care of adults who require ventilation.
- Z-0587-2016 — MOVES System Lithium Polymer Batteries The MOVES System is a portable computer controlled electrically powered transport emergency ventilator intended to provide continuous or intermittent ventilatory support for the care of adults who require ventilation.
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 Thornhill Research, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.