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FDA 510(k)

Nihon Kohden Wireless Input Unit WEE-1200

K-Number: K171124 · 2017-08-25

ApplicantNihon Kohden Corporation
Decision Date2017-08-25
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Nihon Kohden Wireless Input Unit WEE-1200 is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Corporation. It received FDA 510(k) clearance on 2017-08-25 under 510(k) number K171124. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nihon Kohden Wireless Input Unit WEE-1200?

Nihon Kohden Wireless Input Unit WEE-1200 is a medical device that received FDA 510(k) clearance on 2017-08-25. The listed applicant is Nihon Kohden Corporation. The 510(k) number is K171124.

When did Nihon Kohden Wireless Input Unit WEE-1200 receive FDA 510(k) clearance?

Nihon Kohden Wireless Input Unit WEE-1200 received FDA 510(k) clearance on 2017-08-25, under 510(k) number K171124.

Who is the listed applicant for Nihon Kohden Wireless Input Unit WEE-1200?

The FDA 510(k) record lists Nihon Kohden Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nihon Kohden Wireless Input Unit WEE-1200?

The FDA product code for Nihon Kohden Wireless Input Unit WEE-1200 is GWQ.

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Related Devices (Code: GWQ)

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.

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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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