LiquiBand XL

Cutaneous Tissue Adhesive With Mesh

Advanced Medical Solutions Limited

The following data is part of a premarket notification filed by Advanced Medical Solutions Limited with the FDA for Liquiband Xl.

Pre-market Notification Details

Device IDK211878
510k NumberK211878
Device Name:LiquiBand XL
ClassificationCutaneous Tissue Adhesive With Mesh
Applicant Advanced Medical Solutions Limited Western Wood Way , Langage Science Park Plymouth,  GB PL7 5BG
ContactMartin Mitchell
CorrespondentMartin Mitchell
Advanced Medical Solutions Limited Western Wood Way , Langage Science Park Plymouth,  GB PL7 5BG
Product CodeOMD  
CFR Regulation Number878.4011 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-06-21
Decision Date2022-05-23

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
05036912001489 K211878 000
05036912001397 K211878 000
05036912001243 K211878 000

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