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FDA 510(k)

EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS

K-Number: K050032 · 2006-05-17

ApplicantEuromed, Inc.
Decision Date2006-05-17
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS is the device name listed in this FDA 510(k) record. The listed applicant is Euromed, Inc.. It received FDA 510(k) clearance on 2006-05-17 under 510(k) number K050032. 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 EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS?

EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS is a medical device that received FDA 510(k) clearance on 2006-05-17. The listed applicant is Euromed, Inc.. The 510(k) number is K050032.

When did EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS receive FDA 510(k) clearance?

EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS received FDA 510(k) clearance on 2006-05-17, under 510(k) number K050032.

Who is the listed applicant for EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS?

The FDA 510(k) record lists Euromed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS?

The FDA product code for EUROMED SURESKIN III WITH SILVER WOUND DRESSINGS 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 Euromed, Inc. 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.

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

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

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