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FDA 510(k)

TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE

K-Number: K932518 · 1993-10-12

ApplicantConmedcorp
Decision Date1993-10-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1993-10-12 under 510(k) number K932518. 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 TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE?

TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is Conmedcorp. The 510(k) number is K932518.

When did TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE receive FDA 510(k) clearance?

TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE received FDA 510(k) clearance on 1993-10-12, under 510(k) number K932518.

Who is the listed applicant for TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE?

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 TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE?

The FDA product code for TECH-SWITCH ELECTROSURGICAL PENCIL, REUSABLE is GEI.

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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.

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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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