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FDA 510(k)

THE WATER LILY

K-Number: K094022 · 2010-06-11

ApplicantClearwater Products, LLC
Decision Date2010-06-11
Product CodeKPL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THE WATER LILY is the device name listed in this FDA 510(k) record. The listed applicant is Clearwater Products, LLC. It received FDA 510(k) clearance on 2010-06-11 under 510(k) number K094022. The device is classified under product code KPL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE WATER LILY?

THE WATER LILY is a medical device that received FDA 510(k) clearance on 2010-06-11. The listed applicant is Clearwater Products, LLC. The 510(k) number is K094022.

When did THE WATER LILY receive FDA 510(k) clearance?

THE WATER LILY received FDA 510(k) clearance on 2010-06-11, under 510(k) number K094022.

Who is the listed applicant for THE WATER LILY?

The FDA 510(k) record lists Clearwater Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE WATER LILY?

The FDA product code for THE WATER LILY is KPL.

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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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