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FDA 510(k)

DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES

K-Number: K091672 · 2009-12-04

ApplicantShuyou Electric Medical Science Co., Ltd.
Decision Date2009-12-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Shuyou Electric Medical Science Co., Ltd.. It received FDA 510(k) clearance on 2009-12-04 under 510(k) number K091672. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES?

DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES is a medical device that received FDA 510(k) clearance on 2009-12-04. The listed applicant is Shuyou Electric Medical Science Co., Ltd.. The 510(k) number is K091672.

When did DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES receive FDA 510(k) clearance?

DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES received FDA 510(k) clearance on 2009-12-04, under 510(k) number K091672.

Who is the listed applicant for DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES?

The FDA 510(k) record lists Shuyou Electric Medical Science Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES?

The FDA product code for DISPOSABLE GROUNDING PAD SERIES AND ELECTRODE SERIES is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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