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FDA 510(k)

AFM ULTRA AG DRESSINGS

K-Number: K093188 · 2010-02-17

ApplicantMilliken & Co.
Decision Date2010-02-17
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

AFM ULTRA AG DRESSINGS is the device name listed in this FDA 510(k) record. The listed applicant is Milliken & Co.. It received FDA 510(k) clearance on 2010-02-17 under 510(k) number K093188. 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 AFM ULTRA AG DRESSINGS?

AFM ULTRA AG DRESSINGS is a medical device that received FDA 510(k) clearance on 2010-02-17. The listed applicant is Milliken & Co.. The 510(k) number is K093188.

When did AFM ULTRA AG DRESSINGS receive FDA 510(k) clearance?

AFM ULTRA AG DRESSINGS received FDA 510(k) clearance on 2010-02-17, under 510(k) number K093188.

Who is the listed applicant for AFM ULTRA AG DRESSINGS?

The FDA 510(k) record lists Milliken & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AFM ULTRA AG DRESSINGS?

The FDA product code for AFM ULTRA AG DRESSINGS is FRO. This falls under the Anesthesiology category.

Related Clinical Trials

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Other records listing Milliken & Co. 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.

K083659SILVER WOUND PAD

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.

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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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