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FDA 510(k)

Surveyor Patient Monitor

K-Number: K173765 · 2018-09-04

ApplicantMortara Instrument, Inc.
Decision Date2018-09-04
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Surveyor Patient Monitor is a medical device manufactured by Mortara Instrument, Inc.. It received FDA 510(k) clearance on 2018-09-04 under approval number K173765. 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 Surveyor Patient Monitor?

Surveyor Patient Monitor is a medical device that received FDA 510(k) clearance on 2018-09-04. It is manufactured by Mortara Instrument, Inc.. The 510(k) number is K173765.

When was Surveyor Patient Monitor approved by the FDA?

Surveyor Patient Monitor received FDA 510(k) clearance on 2018-09-04, under approval number K173765.

What company makes Surveyor Patient Monitor?

Surveyor Patient Monitor is manufactured by Mortara Instrument, Inc..

What is the FDA product code for Surveyor Patient Monitor?

The FDA product code for Surveyor Patient Monitor is MHX.

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Other Devices by Mortara Instrument, Inc.

K161465CardioConfirm K160685Surveyor S4 Mobile Monitor K152626H3+ Holter Recorder K152944Xscribe Stress Exercise Testing Systems, Q-Stress Stress Exercise Testing Systems K161517Mortara Surveyor Patient Monitor K182297Surveyor S2

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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.

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