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FDA 510(k)

MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS

K-Number: K041884 · 2005-02-28

Decision Date2005-02-28
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Mueller Water Conditioning, Inc.. It received FDA 510(k) clearance on 2005-02-28 under 510(k) number K041884. 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 MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS?

MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS is a medical device that received FDA 510(k) clearance on 2005-02-28. The listed applicant is Mueller Water Conditioning, Inc.. The 510(k) number is K041884.

When did MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS receive FDA 510(k) clearance?

MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS received FDA 510(k) clearance on 2005-02-28, under 510(k) number K041884.

Who is the listed applicant for MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS?

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

What is the FDA product code for MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS?

The FDA product code for MUELLER WATER CONDITIONING WATER PURIFICATION SYSTEM FOR HEMODIALYSIS is FIP.

Related Clinical Trials

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.

Related Devices (Code: FIP)

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.

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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