Decision Date2018-11-30
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
ZOLL Propaq M is a medical device manufactured by ZOLL Medical Corporation. It received FDA 510(k) clearance on 2018-11-30 under approval number K180482. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ZOLL Propaq M?
ZOLL Propaq M is a medical device that received FDA 510(k) clearance on 2018-11-30. It is manufactured by ZOLL Medical Corporation. The 510(k) number is K180482.
When was ZOLL Propaq M approved by the FDA?
ZOLL Propaq M received FDA 510(k) clearance on 2018-11-30, under approval number K180482.
What company makes ZOLL Propaq M?
ZOLL Propaq M is manufactured by ZOLL Medical Corporation.
What is the FDA product code for ZOLL Propaq M?
The FDA product code for ZOLL Propaq M is MHX.
Related Devices (Code: MHX)
K160981Patient MonitorEdan Instruments, Inc.
K153707Nihon Kohden Vital Sign TelemeterNihon Kohden Corporation
K160685Surveyor S4 Mobile MonitorMortara Instrument, Inc.
K161531IntelliVue Patient Monitors MP2, MP5, MP5T, MP5SC, and Multi-Measurement Module X2; IntelliVue Patient Monitors MP20, MP30, MP40, MP50, MP60; IntelliVue Patient Monitors MP70, MP80, MP90;IntelliVue Patient Monitors MX400, MX430, MX450, MX500, MX550, MX600;IntelliVue Patient Monitors MX700, MX800Philips Medizin Systeme Boeblingen GmbH
K153702M3290B Philips IntelliVue Information Center iXPhilips Medical Systems
K160951Philips Efficia CMS200 Central Monitoring SystemPhilips Medical Systems
Official Source
View on FDA Database →
Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.