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FDA 510(k)

ZOLL RESCUENET EPCR MODEL RESCUENET EPCR

K-Number: K103473 · 2011-05-13

ApplicantZOLL Medical Corporation
Decision Date2011-05-13
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOLL RESCUENET EPCR MODEL RESCUENET EPCR 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 2011-05-13 under 510(k) number K103473. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZOLL RESCUENET EPCR MODEL RESCUENET EPCR?

ZOLL RESCUENET EPCR MODEL RESCUENET EPCR is a medical device that received FDA 510(k) clearance on 2011-05-13. The listed applicant is ZOLL Medical Corporation. The 510(k) number is K103473.

When did ZOLL RESCUENET EPCR MODEL RESCUENET EPCR receive FDA 510(k) clearance?

ZOLL RESCUENET EPCR MODEL RESCUENET EPCR received FDA 510(k) clearance on 2011-05-13, under 510(k) number K103473.

Who is the listed applicant for ZOLL RESCUENET EPCR MODEL RESCUENET EPCR?

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 EPCR MODEL RESCUENET EPCR?

The FDA product code for ZOLL RESCUENET EPCR MODEL RESCUENET EPCR is DXJ.

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Other records listing ZOLL Medical Corporation as applicant

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Related Devices (Code: DXJ)

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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