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FDA 510(k)

CONMED ELECTROSURGICAL GROUNDING PAD

K-Number: K954633 · 1995-10-23

ApplicantConmedcorp
Decision Date1995-10-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED ELECTROSURGICAL GROUNDING PAD is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1995-10-23 under 510(k) number K954633. 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 CONMED ELECTROSURGICAL GROUNDING PAD?

CONMED ELECTROSURGICAL GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1995-10-23. The listed applicant is Conmedcorp. The 510(k) number is K954633.

When did CONMED ELECTROSURGICAL GROUNDING PAD receive FDA 510(k) clearance?

CONMED ELECTROSURGICAL GROUNDING PAD received FDA 510(k) clearance on 1995-10-23, under 510(k) number K954633.

Who is the listed applicant for CONMED ELECTROSURGICAL GROUNDING PAD?

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 CONMED ELECTROSURGICAL GROUNDING PAD?

The FDA product code for CONMED ELECTROSURGICAL GROUNDING PAD is GEI.

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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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