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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 a medical device manufactured by Advanced Medical Solutions Limited. It received FDA 510(k) clearance on 2020-03-09 under approval 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. It is manufactured by Advanced Medical Solutions Limited. The 510(k) number is K183570.

When was LiquiBand Plus approved by the FDA?

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

What company makes LiquiBand Plus?

LiquiBand Plus is manufactured by Advanced Medical Solutions Limited.

What is the FDA product code for LiquiBand Plus?

The FDA product code for LiquiBand Plus is MPN.

Other Devices by Advanced Medical Solutions Limited

K211878LiquiBand XL K223310Antimicrobial Silicone PHMB Foam Wound Dressing PMA P220024Tissue adhesive internal use

Related Devices (Code: MPN)

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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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