FDA 510(k)

AQUA PURE DEIONIZER EXCHANGE SERVICE

K-Number: K072158 · 2008-02-21

ApplicantStaubach Barror Water Systems, Inc.

Decision Date2008-02-21

Product CodeFIP

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

AQUA PURE DEIONIZER EXCHANGE SERVICE is the device name listed in this FDA 510(k) record. The listed applicant is Staubach Barror Water Systems, Inc.. It received FDA 510(k) clearance on 2008-02-21 under 510(k) number K072158. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUA PURE DEIONIZER EXCHANGE SERVICE?

AQUA PURE DEIONIZER EXCHANGE SERVICE is a medical device that received FDA 510(k) clearance on 2008-02-21. The listed applicant is Staubach Barror Water Systems, Inc.. The 510(k) number is K072158.

When did AQUA PURE DEIONIZER EXCHANGE SERVICE receive FDA 510(k) clearance?

AQUA PURE DEIONIZER EXCHANGE SERVICE received FDA 510(k) clearance on 2008-02-21, under 510(k) number K072158.

Who is the listed applicant for AQUA PURE DEIONIZER EXCHANGE SERVICE?

The FDA 510(k) record lists Staubach Barror Water Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQUA PURE DEIONIZER EXCHANGE SERVICE?

The FDA product code for AQUA PURE DEIONIZER EXCHANGE SERVICE is FIP.

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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.