Vital Signs Colorado, Inc.
Vital Signs Colorado, Inc. holds FDA 510(k) medical device clearance, cleared in 2005, with 4 FDA device recalls on record.
Top product codes for Vital Signs Colorado, Inc.
FDA recalls by Vital Signs Colorado, Inc.
- Z-1556-2015 — CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation procedure.
- Z-1557-2015 — Introduction Pack. A device inserted into an endotracheal tube to aid in the intubation procedure.
- Z-0812-2014 — Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for use as an interface between a ventilator dependent patient and a ventilator. The Anesthesia Circuit is intended to administer medical gases to a patient during anesthesia. The CPAP Circuit is intended to increase the airway pressure of a patient.
- Z-0407-2013 — Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature
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 Vital Signs Colorado, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.