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FDA 510(k)

TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USE

K-Number: K932345 · 1994-04-12

ApplicantConmedcorp
Decision Date1994-04-12
Product CodeDWG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-04-12 under 510(k) number K932345. The device is classified under product code DWG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USE?

TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USE is a medical device that received FDA 510(k) clearance on 1994-04-12. The listed applicant is Conmedcorp. The 510(k) number is K932345.

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

TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USE received FDA 510(k) clearance on 1994-04-12, under 510(k) number K932345.

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

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, SINGLE USE?

The FDA product code for TECH-SWITCH ELECTROSURGICAL PENCIL, SINGLE USE is DWG.

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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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