Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LiquiBand Plus

K-Number: K183570 · 2020-03-09

ApplicantAdvanced Medical Solutions Limited
Decision Date2020-03-09
Product CodeMPN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LiquiBand Plus 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 2020-03-09 under 510(k) number K183570. 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 Plus?

LiquiBand Plus is a medical device that received FDA 510(k) clearance on 2020-03-09. The listed applicant is Advanced Medical Solutions Limited. The 510(k) number is K183570.

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

LiquiBand Plus received FDA 510(k) clearance on 2020-03-09, under 510(k) number K183570.

Who is the listed applicant for LiquiBand Plus?

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 Plus?

The FDA product code for LiquiBand Plus is MPN.

Related Clinical Trials

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.

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 DressingK211878LiquiBand XLK210974High Performance Antimicrobial Gelling Fiber with SilverK190819Silicone PHMB Foam Wound Dressing

View all 11 devices →

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.

↑