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FDA 510(k)

WATER PURIFIER

K-Number: K001878 · 2000-08-03

ApplicantWaterclave, LLC
Decision Date2000-08-03
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WATER PURIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Waterclave, LLC. It received FDA 510(k) clearance on 2000-08-03 under 510(k) number K001878. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATER PURIFIER?

WATER PURIFIER is a medical device that received FDA 510(k) clearance on 2000-08-03. The listed applicant is Waterclave, LLC. The 510(k) number is K001878.

When did WATER PURIFIER receive FDA 510(k) clearance?

WATER PURIFIER received FDA 510(k) clearance on 2000-08-03, under 510(k) number K001878.

Who is the listed applicant for WATER PURIFIER?

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

What is the FDA product code for WATER PURIFIER?

The FDA product code for WATER PURIFIER is EIA.

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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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