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FDA 510(k)

ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE

K-Number: K072430 · 2007-11-06

ApplicantZOLL Medical Corporation
Decision Date2007-11-06
Product CodeMKJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE 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 2007-11-06 under 510(k) number K072430. The device is classified under product code MKJ. It was reviewed by the CV advisory panel. Product code MKJ falls under the category of Dental, which includes dental instruments, materials, and equipment. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE?

ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE is a medical device that received FDA 510(k) clearance on 2007-11-06. The listed applicant is ZOLL Medical Corporation. The 510(k) number is K072430.

When did ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE receive FDA 510(k) clearance?

ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE received FDA 510(k) clearance on 2007-11-06, under 510(k) number K072430.

Who is the listed applicant for ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE?

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 PEDIPADZ REDUCED ENERGY ELECTRODE?

The FDA product code for ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE is MKJ. This falls under the Dental category.

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Related Devices (Code: MKJ)

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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