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FDA 510(k)

NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM

K-Number: K001811 · 2000-10-25

ApplicantNeu-Ion, Inc.
Decision Date2000-10-25
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Neu-Ion, Inc.. It received FDA 510(k) clearance on 2000-10-25 under 510(k) number K001811. 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 NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM?

NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2000-10-25. The listed applicant is Neu-Ion, Inc.. The 510(k) number is K001811.

When did NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM receive FDA 510(k) clearance?

NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM received FDA 510(k) clearance on 2000-10-25, under 510(k) number K001811.

Who is the listed applicant for NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM?

The FDA 510(k) record lists Neu-Ion, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEU-ION HEMODIALYIS WATER TREATMENT SYSTEM?

The FDA product code for NEU-ION HEMODIALYIS WATER TREATMENT 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.

K250471AquaC UNO HFresenius Medical Care Renal Therapies Group, LLCK251851DIASAFEplusUS (F00013010)Fresenius Medical Care Renal Therapies Group, LLCK252181AquaAFresenius Medical Care North AmericaK250514UPT Series Medical RO Water Treatment SystemSpecialty Water Technologies, Inc.K232953AquaBplus; AquaB LITEFresenius Medical Care Renal Therapies Group, LLCK223479AQUAbase nXB.Braun Medical, Inc.

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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