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FDA 510(k)

LIQUIBAND ULTIMA, MODEL LB0004

K-Number: K083531 · 2009-02-12

ApplicantMedlogic Global , Ltd.
Decision Date2009-02-12
Product CodeMPN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIQUIBAND ULTIMA, MODEL LB0004 is the device name listed in this FDA 510(k) record. The listed applicant is Medlogic Global , Ltd.. It received FDA 510(k) clearance on 2009-02-12 under 510(k) number K083531. The device is classified under product code MPN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUIBAND ULTIMA, MODEL LB0004?

LIQUIBAND ULTIMA, MODEL LB0004 is a medical device that received FDA 510(k) clearance on 2009-02-12. The listed applicant is Medlogic Global , Ltd.. The 510(k) number is K083531.

When did LIQUIBAND ULTIMA, MODEL LB0004 receive FDA 510(k) clearance?

LIQUIBAND ULTIMA, MODEL LB0004 received FDA 510(k) clearance on 2009-02-12, under 510(k) number K083531.

Who is the listed applicant for LIQUIBAND ULTIMA, MODEL LB0004?

The FDA 510(k) record lists Medlogic Global , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUIBAND ULTIMA, MODEL LB0004?

The FDA product code for LIQUIBAND ULTIMA, MODEL LB0004 is MPN.

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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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