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FDA 510(k)

LIXIVITRON

K-Number: K802828 · 1981-05-08

ApplicantUnited Medical
Decision Date1981-05-08
Product CodeLIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LIXIVITRON is the device name listed in this FDA 510(k) record. The listed applicant is United Medical. It received FDA 510(k) clearance on 1981-05-08 under 510(k) number K802828. The device is classified under product code LIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIXIVITRON?

LIXIVITRON is a medical device that received FDA 510(k) clearance on 1981-05-08. The listed applicant is United Medical. The 510(k) number is K802828.

When did LIXIVITRON receive FDA 510(k) clearance?

LIXIVITRON received FDA 510(k) clearance on 1981-05-08, under 510(k) number K802828.

Who is the listed applicant for LIXIVITRON?

The FDA 510(k) record lists United Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIXIVITRON?

The FDA product code for LIXIVITRON is LIF.

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.

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Other records listing United Medical as applicant

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.

K883849REPLICARE (ADDITIONAL CLAIMS)K880299REPLICAREK863389UNITED WOUND COVERING, PACKAGE OF 5

Related Devices (Code: LIF)

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.

K091360CLEARFLUX DIALYZER REPROCESSING SYSTEMNovaflux TechnologiesK043126ASSIST HEADER CLEANERAlcavis International, Inc.K040660STERICHEK GLUTARALDEHYDE REAGENT STRIPSHach CompanyK033505RENACLEAN SH DIALYZER CLEANING SYSTEMMinntech Corp.K024076MAKY 21.1 DIALYZER REPROCESSING SYSTEMHdc Maquinolas, LLCK013713ARM AUTOMATIC REPROCESSING MACHINEAlcavis International Incorporated

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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