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FDA 510(k)

ELECTROSURGICAL GROUND PAD-DISPERSIVE

K-Number: K830613 · 1983-04-12

Decision Date1983-04-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL GROUND PAD-DISPERSIVE is the device name listed in this FDA 510(k) record. The listed applicant is Con Med Equipment, Inc.. It received FDA 510(k) clearance on 1983-04-12 under 510(k) number K830613. 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 ELECTROSURGICAL GROUND PAD-DISPERSIVE?

ELECTROSURGICAL GROUND PAD-DISPERSIVE is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Con Med Equipment, Inc.. The 510(k) number is K830613.

When did ELECTROSURGICAL GROUND PAD-DISPERSIVE receive FDA 510(k) clearance?

ELECTROSURGICAL GROUND PAD-DISPERSIVE received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830613.

Who is the listed applicant for ELECTROSURGICAL GROUND PAD-DISPERSIVE?

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

What is the FDA product code for ELECTROSURGICAL GROUND PAD-DISPERSIVE?

The FDA product code for ELECTROSURGICAL GROUND PAD-DISPERSIVE 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 Con Med Equipment, 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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