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FDA 510(k)

GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR

K-Number: K043352 · 2005-03-31

ApplicantGocanning Technology , Ltd.
Decision Date2005-03-31
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Gocanning Technology , Ltd.. It received FDA 510(k) clearance on 2005-03-31 under 510(k) number K043352. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR?

GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR is a medical device that received FDA 510(k) clearance on 2005-03-31. The listed applicant is Gocanning Technology , Ltd.. The 510(k) number is K043352.

When did GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR receive FDA 510(k) clearance?

GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR received FDA 510(k) clearance on 2005-03-31, under 510(k) number K043352.

Who is the listed applicant for GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR?

The FDA 510(k) record lists Gocanning Technology , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR?

The FDA product code for GOCANNING GLS-700 E-PULSE ANALYSIS MONITOR is DXN.

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Related Devices (Code: DXN)

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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