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FDA 510(k)

Critical Alert CommonPath Enterprise

K-Number: K193043 · 2020-05-11

ApplicantCritical Alert
Decision Date2020-05-11
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Critical Alert CommonPath Enterprise is the device name listed in this FDA 510(k) record. The listed applicant is Critical Alert. It received FDA 510(k) clearance on 2020-05-11 under 510(k) number K193043. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Critical Alert CommonPath Enterprise?

Critical Alert CommonPath Enterprise is a medical device that received FDA 510(k) clearance on 2020-05-11. The listed applicant is Critical Alert. The 510(k) number is K193043.

When did Critical Alert CommonPath Enterprise receive FDA 510(k) clearance?

Critical Alert CommonPath Enterprise received FDA 510(k) clearance on 2020-05-11, under 510(k) number K193043.

Who is the listed applicant for Critical Alert CommonPath Enterprise?

The FDA 510(k) record lists Critical Alert as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Critical Alert CommonPath Enterprise?

The FDA product code for Critical Alert CommonPath Enterprise is MSX.

Related Devices (Code: MSX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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