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FDA 510(k)

TARGET STERILE ELECTRODE

K-Number: K072799 · 2008-04-24

ApplicantVision Quest Industries, Inc.
Decision Date2008-04-24
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TARGET STERILE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Vision Quest Industries, Inc.. It received FDA 510(k) clearance on 2008-04-24 under 510(k) number K072799. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARGET STERILE ELECTRODE?

TARGET STERILE ELECTRODE is a medical device that received FDA 510(k) clearance on 2008-04-24. The listed applicant is Vision Quest Industries, Inc.. The 510(k) number is K072799.

When did TARGET STERILE ELECTRODE receive FDA 510(k) clearance?

TARGET STERILE ELECTRODE received FDA 510(k) clearance on 2008-04-24, under 510(k) number K072799.

Who is the listed applicant for TARGET STERILE ELECTRODE?

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

What is the FDA product code for TARGET STERILE ELECTRODE?

The FDA product code for TARGET STERILE ELECTRODE is GXY.

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Other records listing Vision Quest Industries, 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.

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Related Devices (Code: GXY)

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.

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Official Source

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