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FDA 510(k)

ELECTRO SENSOR -BODY COMPOSITION

K-Number: K103026 · 2011-03-29

Decision Date2011-03-29
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRO SENSOR -BODY COMPOSITION 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 2011-03-29 under 510(k) number K103026. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO SENSOR -BODY COMPOSITION?

ELECTRO SENSOR -BODY COMPOSITION is a medical device that received FDA 510(k) clearance on 2011-03-29. The listed applicant is Ld Technology, LLC. The 510(k) number is K103026.

When did ELECTRO SENSOR -BODY COMPOSITION receive FDA 510(k) clearance?

ELECTRO SENSOR -BODY COMPOSITION received FDA 510(k) clearance on 2011-03-29, under 510(k) number K103026.

Who is the listed applicant for ELECTRO SENSOR -BODY COMPOSITION?

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 -BODY COMPOSITION?

The FDA product code for ELECTRO SENSOR -BODY COMPOSITION is MNW.

Related Clinical Trials

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.

Other records listing Ld Technology, LLC 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.

View all 11 devices →

Related Devices (Code: MNW)

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.

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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