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FDA 510(k)

Disposable Snap Electrode

K-Number: K172703 · 2017-11-13

ApplicantEmbla Systems
Decision Date2017-11-13
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Disposable Snap Electrode is the device name listed in this FDA 510(k) record. The listed applicant is Embla Systems. It received FDA 510(k) clearance on 2017-11-13 under 510(k) number K172703. 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 Disposable Snap Electrode?

Disposable Snap Electrode is a medical device that received FDA 510(k) clearance on 2017-11-13. The listed applicant is Embla Systems. The 510(k) number is K172703.

When did Disposable Snap Electrode receive FDA 510(k) clearance?

Disposable Snap Electrode received FDA 510(k) clearance on 2017-11-13, under 510(k) number K172703.

Who is the listed applicant for Disposable Snap Electrode?

The FDA 510(k) record lists Embla Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Snap Electrode?

The FDA product code for Disposable Snap Electrode is GXY.

Other records listing Embla Systems 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.

K180001Disposable BreathSensor Adult, Disposable BreathSensor Small Adult / Child, Disposable BreathSensor Preemie, Disposable BreathSensor InfantK173793XactTrace Single Use Respiratory Effort Belt SystemK163617REMbrandtK162140RemLogicK153353SANDMAN ELITE

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

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