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FDA 510(k)

MPW HEMODIALYSIS WATER PURIFICATION SYSTEM

K-Number: K001755 · 2002-08-05

ApplicantMpw Industrial Water Services, Inc.
Decision Date2002-08-05
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MPW HEMODIALYSIS WATER PURIFICATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mpw Industrial Water Services, Inc.. It received FDA 510(k) clearance on 2002-08-05 under 510(k) number K001755. 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 MPW HEMODIALYSIS WATER PURIFICATION SYSTEM?

MPW HEMODIALYSIS WATER PURIFICATION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-08-05. The listed applicant is Mpw Industrial Water Services, Inc.. The 510(k) number is K001755.

When did MPW HEMODIALYSIS WATER PURIFICATION SYSTEM receive FDA 510(k) clearance?

MPW HEMODIALYSIS WATER PURIFICATION SYSTEM received FDA 510(k) clearance on 2002-08-05, under 510(k) number K001755.

Who is the listed applicant for MPW HEMODIALYSIS WATER PURIFICATION SYSTEM?

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

What is the FDA product code for MPW HEMODIALYSIS WATER PURIFICATION SYSTEM?

The FDA product code for MPW HEMODIALYSIS WATER PURIFICATION SYSTEM is FIP.

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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.

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Official Source

View on FDA Database →

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

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