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FDA 510(k)

HEMODIAL CONCENTRATE MIXING APPARATUS

K-Number: K842225 · 1984-10-02

ApplicantLmf Medical Research & Manufacturing, Inc.
Decision Date1984-10-02
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEMODIAL CONCENTRATE MIXING APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Lmf Medical Research & Manufacturing, Inc.. It received FDA 510(k) clearance on 1984-10-02 under 510(k) number K842225. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMODIAL CONCENTRATE MIXING APPARATUS?

HEMODIAL CONCENTRATE MIXING APPARATUS is a medical device that received FDA 510(k) clearance on 1984-10-02. The listed applicant is Lmf Medical Research & Manufacturing, Inc.. The 510(k) number is K842225.

When did HEMODIAL CONCENTRATE MIXING APPARATUS receive FDA 510(k) clearance?

HEMODIAL CONCENTRATE MIXING APPARATUS received FDA 510(k) clearance on 1984-10-02, under 510(k) number K842225.

Who is the listed applicant for HEMODIAL CONCENTRATE MIXING APPARATUS?

The FDA 510(k) record lists Lmf Medical Research & Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMODIAL CONCENTRATE MIXING APPARATUS?

The FDA product code for HEMODIAL CONCENTRATE MIXING APPARATUS is FKQ.

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Related Devices (Code: FKQ)

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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