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FDA 510(k)

ZOLL PROPAQ XM

K-Number: K121367 · 2012-06-21

ApplicantZOLL Medical Corporation
Decision Date2012-06-21
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOLL PROPAQ XM is the device name listed in this FDA 510(k) record. The listed applicant is ZOLL Medical Corporation. It received FDA 510(k) clearance on 2012-06-21 under 510(k) number K121367. 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 XM?

ZOLL PROPAQ XM is a medical device that received FDA 510(k) clearance on 2012-06-21. The listed applicant is ZOLL Medical Corporation. The 510(k) number is K121367.

When did ZOLL PROPAQ XM receive FDA 510(k) clearance?

ZOLL PROPAQ XM received FDA 510(k) clearance on 2012-06-21, under 510(k) number K121367.

Who is the listed applicant for ZOLL PROPAQ XM?

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

What is the FDA product code for ZOLL PROPAQ XM?

The FDA product code for ZOLL PROPAQ XM is MHX.

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Other records listing ZOLL Medical Corporation as applicant

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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Related Devices (Code: MHX)

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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