IP Converter
K-Number: K191678 · 2020-01-10
Device Summary
Frequently Asked Questions
What is the IP Converter?
IP Converter is a medical device that received FDA 510(k) clearance on 2020-01-10. The listed applicant is Sony Electronics, Inc.. The 510(k) number is K191678.
When did IP Converter receive FDA 510(k) clearance?
IP Converter received FDA 510(k) clearance on 2020-01-10, under 510(k) number K191678.
Who is the listed applicant for IP Converter?
The FDA 510(k) record lists Sony Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IP Converter?
The FDA product code for IP Converter is GCJ.
Other records listing Sony Electronics, Inc. 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.
Related Devices (Code: GCJ)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.