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FDA 510(k)

D function

K-Number: K203525 · 2021-05-05

ApplicantIto Co., Ltd.
Decision Date2021-05-05
Product CodeNUW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

D function is the device name listed in this FDA 510(k) record. The listed applicant is Ito Co., Ltd.. It received FDA 510(k) clearance on 2021-05-05 under 510(k) number K203525. The device is classified under product code NUW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D function?

D function is a medical device that received FDA 510(k) clearance on 2021-05-05. The listed applicant is Ito Co., Ltd.. The 510(k) number is K203525.

When did D function receive FDA 510(k) clearance?

D function received FDA 510(k) clearance on 2021-05-05, under 510(k) number K203525.

Who is the listed applicant for D function?

The FDA 510(k) record lists Ito Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for D function?

The FDA product code for D function is NUW.

Related Devices (Code: NUW)

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.

K243290BTL-785MJBTL Industries, Inc.

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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