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FDA 510(k)

WWMED, MODEL 401

K-Number: K051961 · 2006-02-10

ApplicantWong Way Corporation
Decision Date2006-02-10
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WWMED, MODEL 401 is the device name listed in this FDA 510(k) record. The listed applicant is Wong Way Corporation. It received FDA 510(k) clearance on 2006-02-10 under 510(k) number K051961. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WWMED, MODEL 401?

WWMED, MODEL 401 is a medical device that received FDA 510(k) clearance on 2006-02-10. The listed applicant is Wong Way Corporation. The 510(k) number is K051961.

When did WWMED, MODEL 401 receive FDA 510(k) clearance?

WWMED, MODEL 401 received FDA 510(k) clearance on 2006-02-10, under 510(k) number K051961.

Who is the listed applicant for WWMED, MODEL 401?

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

What is the FDA product code for WWMED, MODEL 401?

The FDA product code for WWMED, MODEL 401 is ILY.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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