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FDA 510(k)

ZOLL RESCUENET 12-LEAD

K-Number: K121865 · 2012-11-20

ApplicantZOLL Medical Corporation
Decision Date2012-11-20
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOLL RESCUENET 12-LEAD 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 2012-11-20 under 510(k) number K121865. 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 ZOLL RESCUENET 12-LEAD?

ZOLL RESCUENET 12-LEAD is a medical device that received FDA 510(k) clearance on 2012-11-20. The listed applicant is ZOLL Medical Corporation. The 510(k) number is K121865.

When did ZOLL RESCUENET 12-LEAD receive FDA 510(k) clearance?

ZOLL RESCUENET 12-LEAD received FDA 510(k) clearance on 2012-11-20, under 510(k) number K121865.

Who is the listed applicant for ZOLL RESCUENET 12-LEAD?

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 RESCUENET 12-LEAD?

The FDA product code for ZOLL RESCUENET 12-LEAD is MSX.

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Related Devices (Code: MSX)

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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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