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FDA 510(k)

SILVER ANTIMICROBIAL WOUND GEL

K-Number: K110458 · 2011-03-14

Decision Date2011-03-14
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

SILVER ANTIMICROBIAL WOUND GEL 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 2011-03-14 under 510(k) number K110458. 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 SILVER ANTIMICROBIAL WOUND GEL?

SILVER ANTIMICROBIAL WOUND GEL is a medical device that received FDA 510(k) clearance on 2011-03-14. The listed applicant is Advanced Medical Solutions Limited. The 510(k) number is K110458.

When did SILVER ANTIMICROBIAL WOUND GEL receive FDA 510(k) clearance?

SILVER ANTIMICROBIAL WOUND GEL received FDA 510(k) clearance on 2011-03-14, under 510(k) number K110458.

Who is the listed applicant for SILVER ANTIMICROBIAL WOUND GEL?

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 SILVER ANTIMICROBIAL WOUND GEL?

The FDA product code for SILVER ANTIMICROBIAL WOUND GEL is FRO. This falls under the Anesthesiology category.

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.

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.

View all 11 devices →

Related Devices (Code: FRO)

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.

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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