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FDA 510(k)

LIQUIBAND DUAL, MODEL LBD 001

K-Number: K102076 · 2011-02-18

ApplicantMedlogic Global Limited
Decision Date2011-02-18
Product CodeMPN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIQUIBAND DUAL, MODEL LBD 001 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 2011-02-18 under 510(k) number K102076. 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 DUAL, MODEL LBD 001?

LIQUIBAND DUAL, MODEL LBD 001 is a medical device that received FDA 510(k) clearance on 2011-02-18. The listed applicant is Medlogic Global Limited. The 510(k) number is K102076.

When did LIQUIBAND DUAL, MODEL LBD 001 receive FDA 510(k) clearance?

LIQUIBAND DUAL, MODEL LBD 001 received FDA 510(k) clearance on 2011-02-18, under 510(k) number K102076.

Who is the listed applicant for LIQUIBAND DUAL, MODEL LBD 001?

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 DUAL, MODEL LBD 001?

The FDA product code for LIQUIBAND DUAL, MODEL LBD 001 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 CONTROLK100284LIQUIBAND ULTIMA, LUT 003K031321LIQUISHIELD 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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