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FDA 510(k)

ZOLL Propaq M

K-Number: K180482 · 2018-11-30

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.

Other Devices by ZOLL Medical Corporation

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Related Devices (Code: MHX)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.