Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Embla Systems. It received FDA 510(k) clearance on 2017-11-13 under approval 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. It is manufactured by Embla Systems. The 510(k) number is K172703.

When was Disposable Snap Electrode approved by the FDA?

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

What company makes Disposable Snap Electrode?

Disposable Snap Electrode is manufactured by Embla Systems.

What is the FDA product code for Disposable Snap Electrode?

The FDA product code for Disposable Snap Electrode is GXY.

Other Devices by Embla Systems

Related Devices (Code: GXY)

Official Source

View on FDA Database →

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