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FDA 510(k)

IP Converter

K-Number: K191678 · 2020-01-10

ApplicantSony Electronics, Inc.
Decision Date2020-01-10
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

IP Converter is a medical device manufactured by Sony Electronics, Inc.. It received FDA 510(k) clearance on 2020-01-10 under approval number K191678. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IP Converter?

IP Converter is a medical device that received FDA 510(k) clearance on 2020-01-10. It is manufactured by Sony Electronics, Inc.. The 510(k) number is K191678.

When was IP Converter approved by the FDA?

IP Converter received FDA 510(k) clearance on 2020-01-10, under approval number K191678.

What company makes IP Converter?

IP Converter is manufactured by Sony Electronics, Inc..

What is the FDA product code for IP Converter?

The FDA product code for IP Converter is GCJ.

Other Devices by Sony Electronics, Inc.

K161122Sony IP Converter NU-IP40S

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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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