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FDA 510(k)

LD-Oxi system

K-Number: K160956 · 2016-07-06

ApplicantLd Technology, LLC
Decision Date2016-07-06
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LD-Oxi system is a medical device manufactured by Ld Technology, LLC. It received FDA 510(k) clearance on 2016-07-06 under approval number K160956. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LD-Oxi system?

LD-Oxi system is a medical device that received FDA 510(k) clearance on 2016-07-06. It is manufactured by Ld Technology, LLC. The 510(k) number is K160956.

When was LD-Oxi system approved by the FDA?

LD-Oxi system received FDA 510(k) clearance on 2016-07-06, under approval number K160956.

What company makes LD-Oxi system?

LD-Oxi system is manufactured by Ld Technology, LLC.

What is the FDA product code for LD-Oxi system?

The FDA product code for LD-Oxi system is MWI.

Other Devices by Ld Technology, LLC

K173696TBL-ABI System K200287BP-BT Kiosk K200141Oxi-W System

Related Devices (Code: MWI)

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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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