FDA 510(k)

Model WP-3840 and WP-3040

K-Number: K173848 · 2018-08-07

Decision Date2018-08-07

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Model WP-3840 and WP-3040 is the device name listed in this FDA 510(k) record. The listed applicant is Cnmc Co., Inc.. It received FDA 510(k) clearance on 2018-08-07 under 510(k) number K173848. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Model WP-3840 and WP-3040?

Model WP-3840 and WP-3040 is a medical device that received FDA 510(k) clearance on 2018-08-07. The listed applicant is Cnmc Co., Inc.. The 510(k) number is K173848.

When did Model WP-3840 and WP-3040 receive FDA 510(k) clearance?

Model WP-3840 and WP-3040 received FDA 510(k) clearance on 2018-08-07, under 510(k) number K173848.

Who is the listed applicant for Model WP-3840 and WP-3040?

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

What is the FDA product code for Model WP-3840 and WP-3040?

The FDA product code for Model WP-3840 and WP-3040 is IYE.

Related Devices (Code: IYE)

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

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