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FDA 510(k)

ELECTROSURGICAL PENCILS

K-Number: K040780 · 2005-02-10

Decision Date2005-02-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL PENCILS is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Shuyou Medical Instrument Company, Ltd.. It received FDA 510(k) clearance on 2005-02-10 under 510(k) number K040780. 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 ELECTROSURGICAL PENCILS?

ELECTROSURGICAL PENCILS is a medical device that received FDA 510(k) clearance on 2005-02-10. The listed applicant is Hangzhou Shuyou Medical Instrument Company, Ltd.. The 510(k) number is K040780.

When did ELECTROSURGICAL PENCILS receive FDA 510(k) clearance?

ELECTROSURGICAL PENCILS received FDA 510(k) clearance on 2005-02-10, under 510(k) number K040780.

Who is the listed applicant for ELECTROSURGICAL PENCILS?

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

What is the FDA product code for ELECTROSURGICAL PENCILS?

The FDA product code for ELECTROSURGICAL PENCILS is GEI.

Related Clinical Trials

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.

Related Devices (Code: GEI)

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.

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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