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FDA 510(k)

LIQUIBAND ULTIMA, LUT 003

K-Number: K100284 · 2010-04-09

ApplicantMedlogic Global Limited
Decision Date2010-04-09
Product CodeMPN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIQUIBAND ULTIMA, LUT 003 is the device name listed in this FDA 510(k) record. The listed applicant is Medlogic Global Limited. It received FDA 510(k) clearance on 2010-04-09 under 510(k) number K100284. 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, LUT 003?

LIQUIBAND ULTIMA, LUT 003 is a medical device that received FDA 510(k) clearance on 2010-04-09. The listed applicant is Medlogic Global Limited. The 510(k) number is K100284.

When did LIQUIBAND ULTIMA, LUT 003 receive FDA 510(k) clearance?

LIQUIBAND ULTIMA, LUT 003 received FDA 510(k) clearance on 2010-04-09, under 510(k) number K100284.

Who is the listed applicant for LIQUIBAND ULTIMA, LUT 003?

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

What is the FDA product code for LIQUIBAND ULTIMA, LUT 003?

The FDA product code for LIQUIBAND ULTIMA, LUT 003 is MPN.

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Other records listing Medlogic Global Limited 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.

K110184LIQUIBAND FLOW CONTROLK102076LIQUIBAND DUAL, MODEL LBD 001K031321LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001K023163LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020

Related Devices (Code: MPN)

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.

K243990BondEase 2 Topical Skin AdhesiveOptmed, Inc.K250950CUTIVA™ Topical Skin Adhesive (RM1700); CUTIVA™ PLUS Skin Closure System (RM1739)Okapi Medical, LLC Dba Resivant MedicalK234114CUTIVA(TM) Topical Skin Adhesive (RM-1700); CUTIVA(TM) PLUS Skin Closure System (RM-1739)Okapi Medical, LLC Dba Resivant MedicalK233458CM005 Standard (CM005); CM004 Mini (CM004)Connexicon Medical , Ltd.K230981Meriglu Topical Skin AdhesiveM/s. Meril Endo Surgery Private Limited.K212246Exofin Precision PenChemence Medical, Inc.

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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