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FDA 510(k)

LiquiBand XL

K-Number: K211878 · 2022-05-23

ApplicantAdvanced Medical Solutions Limited
Decision Date2022-05-23
Product CodeOMD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LiquiBand XL is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Solutions Limited. It received FDA 510(k) clearance on 2022-05-23 under 510(k) number K211878. The device is classified under product code OMD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LiquiBand XL?

LiquiBand XL is a medical device that received FDA 510(k) clearance on 2022-05-23. The listed applicant is Advanced Medical Solutions Limited. The 510(k) number is K211878.

When did LiquiBand XL receive FDA 510(k) clearance?

LiquiBand XL received FDA 510(k) clearance on 2022-05-23, under 510(k) number K211878.

Who is the listed applicant for LiquiBand XL?

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

What is the FDA product code for LiquiBand XL?

The FDA product code for LiquiBand XL is OMD.

Related Clinical Trials

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NCT07255937PMCF Study of Debridement PadCOMPLETEDNCT07295379LIQUIBAND FIX8® for Ventral Incisional HerniaACTIVE_NOT_RECRUITING

Other records listing Advanced Medical Solutions 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.

PMA P220024Tissue adhesive internal useK213473Antimicrobial Gelling Fiber Dressing with PHMBK223310Antimicrobial Silicone PHMB Foam Wound DressingK210974High Performance Antimicrobial Gelling Fiber with SilverK183570LiquiBand PlusK190819Silicone PHMB Foam Wound Dressing

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Related Devices (Code: OMD)

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.

K233460CM00622 LINC Skin Closure System (CM00622 LINC)Connexicon Medical , Ltd.K213512DERMABOND PRINEO Skin Closure SystemETHICON, Inc.K191461Exofin Fusion Skin Closure SystemChemence Medical, Inc.K171442Exofin Fusion Skin Closure SystemChemence Medical, Inc.K163645DERMABOND PRINEO Skin Closure SystemEthicon, LLC

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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