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FDA 510(k)

PHMB Foam Wound Dressing

K-Number: K181197 · 2018-08-03

Decision Date2018-08-03
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

PHMB Foam Wound Dressing is a medical device manufactured by Advanced Medical Solutions, Ltd.. It received FDA 510(k) clearance on 2018-08-03 under approval number K181197. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHMB Foam Wound Dressing?

PHMB Foam Wound Dressing is a medical device that received FDA 510(k) clearance on 2018-08-03. It is manufactured by Advanced Medical Solutions, Ltd.. The 510(k) number is K181197.

When was PHMB Foam Wound Dressing approved by the FDA?

PHMB Foam Wound Dressing received FDA 510(k) clearance on 2018-08-03, under approval number K181197.

What company makes PHMB Foam Wound Dressing?

PHMB Foam Wound Dressing is manufactured by Advanced Medical Solutions, Ltd..

What is the FDA product code for PHMB Foam Wound Dressing?

The FDA product code for PHMB Foam Wound Dressing is FRO. This falls under the Anesthesiology category.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.