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FDA 510(k)

MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES

K-Number: K936246 · 1994-07-21

Decision Date1994-07-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Medicon Instruments, Inc.. It received FDA 510(k) clearance on 1994-07-21 under 510(k) number K936246. 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 MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES?

MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-07-21. The listed applicant is Medicon Instruments, Inc.. The 510(k) number is K936246.

When did MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES receive FDA 510(k) clearance?

MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES received FDA 510(k) clearance on 1994-07-21, under 510(k) number K936246.

Who is the listed applicant for MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES?

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

What is the FDA product code for MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES?

The FDA product code for MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES 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 Medicon Instruments, Inc. 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.

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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