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FDA 510(k)

CONMED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS

K-Number: K934656 · 1994-02-17

ApplicantConmedcorp
Decision Date1994-02-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K934656. 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 CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS?

CONMED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Conmedcorp. The 510(k) number is K934656.

When did CONMED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS receive FDA 510(k) clearance?

CONMED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS received FDA 510(k) clearance on 1994-02-17, under 510(k) number K934656.

Who is the listed applicant for CONMED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS?

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 CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS?

The FDA product code for CONMED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNDING PADS is GEI.

Related Clinical Trials

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.

Other records listing Conmedcorp as applicant

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.

View all 92 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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