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FDA 510(k)

LIQUIBAND FLOW CONTROL

K-Number: K110184 · 2011-12-16

ApplicantMedlogic Global Limited
Decision Date2011-12-16
Product CodeMPN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIQUIBAND FLOW CONTROL 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 2011-12-16 under 510(k) number K110184. 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 FLOW CONTROL?

LIQUIBAND FLOW CONTROL is a medical device that received FDA 510(k) clearance on 2011-12-16. The listed applicant is Medlogic Global Limited. The 510(k) number is K110184.

When did LIQUIBAND FLOW CONTROL receive FDA 510(k) clearance?

LIQUIBAND FLOW CONTROL received FDA 510(k) clearance on 2011-12-16, under 510(k) number K110184.

Who is the listed applicant for LIQUIBAND FLOW CONTROL?

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 FLOW CONTROL?

The FDA product code for LIQUIBAND FLOW CONTROL 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.

K102076LIQUIBAND DUAL, MODEL LBD 001K100284LIQUIBAND 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

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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