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FDA 510(k)

ELECTRO-SURGICAL PENCILS

K-Number: K861742 · 1986-07-23

ApplicantStryker Corp.
Decision Date1986-07-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRO-SURGICAL PENCILS is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1986-07-23 under 510(k) number K861742. 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 ELECTRO-SURGICAL PENCILS?

ELECTRO-SURGICAL PENCILS is a medical device that received FDA 510(k) clearance on 1986-07-23. The listed applicant is Stryker Corp.. The 510(k) number is K861742.

When did ELECTRO-SURGICAL PENCILS receive FDA 510(k) clearance?

ELECTRO-SURGICAL PENCILS received FDA 510(k) clearance on 1986-07-23, under 510(k) number K861742.

Who is the listed applicant for ELECTRO-SURGICAL PENCILS?

The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRO-SURGICAL PENCILS?

The FDA product code for ELECTRO-SURGICAL PENCILS is GEI.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: GEI)

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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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