FDA 510(k)

ZOLL Propaq M

K-Number: K202375 · 2021-03-09

Decision Date2021-03-09

Product CodeMWI

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 2021-03-09 under approval number K202375. The device is classified under product code MWI. 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 2021-03-09. It is manufactured by ZOLL Medical Corporation. The 510(k) number is K202375.

When was ZOLL Propaq M approved by the FDA?

ZOLL Propaq M received FDA 510(k) clearance on 2021-03-09, under approval number K202375.

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 MWI.

Other Devices by ZOLL Medical Corporation

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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.