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FDA 510(k)

ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)

K-Number: K113264 · 2012-03-02

ApplicantLd Technology, LLC
Decision Date2012-03-02
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE) is the device name listed in this FDA 510(k) record. The listed applicant is Ld Technology, LLC. It received FDA 510(k) clearance on 2012-03-02 under 510(k) number K113264. 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 ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)?

ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE) is a medical device that received FDA 510(k) clearance on 2012-03-02. The listed applicant is Ld Technology, LLC. The 510(k) number is K113264.

When did ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE) receive FDA 510(k) clearance?

ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE) received FDA 510(k) clearance on 2012-03-02, under 510(k) number K113264.

Who is the listed applicant for ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)?

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

What is the FDA product code for ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)?

The FDA product code for ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE) is DXN.

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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.

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