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FDA 510(k)

HAND CONTROLLED ELECTROSURGICAL PENCILS

K-Number: K896626 · 1990-01-11

ApplicantConmedcorp
Decision Date1990-01-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HAND CONTROLLED ELECTROSURGICAL PENCILS is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1990-01-11 under 510(k) number K896626. 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 HAND CONTROLLED ELECTROSURGICAL PENCILS?

HAND CONTROLLED ELECTROSURGICAL PENCILS is a medical device that received FDA 510(k) clearance on 1990-01-11. The listed applicant is Conmedcorp. The 510(k) number is K896626.

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

HAND CONTROLLED ELECTROSURGICAL PENCILS received FDA 510(k) clearance on 1990-01-11, under 510(k) number K896626.

Who is the listed applicant for HAND CONTROLLED ELECTROSURGICAL PENCILS?

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

What is the FDA product code for HAND CONTROLLED ELECTROSURGICAL PENCILS?

The FDA product code for HAND CONTROLLED ELECTROSURGICAL PENCILS is 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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