Belmont Instrument Corporation
Belmont Instrument Corporation holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2015, with 2 FDA device recalls on record.
Top product codes for Belmont Instrument Corporation
FDA recalls by Belmont Instrument Corporation
- Z-0153-2023 — CritiCool, thermoregulation device
- Z-0058-2013 — Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
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 Belmont Instrument Corporation
Data sourced from openFDA. This site is unofficial and independent of the FDA.