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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 a medical device manufactured by Advanced Medical Solutions Limited. It received FDA 510(k) clearance on 2022-05-23 under approval 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. It is manufactured by Advanced Medical Solutions Limited. The 510(k) number is K211878.

When was LiquiBand XL approved by the FDA?

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

What company makes LiquiBand XL?

LiquiBand XL is manufactured by Advanced Medical Solutions Limited.

What is the FDA product code for LiquiBand XL?

The FDA product code for LiquiBand XL is OMD.

Other Devices by Advanced Medical Solutions Limited

K183570LiquiBand Plus K223310Antimicrobial Silicone PHMB Foam Wound Dressing PMA P220024Tissue adhesive internal use

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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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