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FDA 510(k)

SILVERLON CONTACT WOUND DRESSING

K-Number: K981299 · 1998-09-25

Decision Date1998-09-25
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

SILVERLON CONTACT WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Argentum International, LLC. It received FDA 510(k) clearance on 1998-09-25 under 510(k) number K981299. 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 SILVERLON CONTACT WOUND DRESSING?

SILVERLON CONTACT WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1998-09-25. The listed applicant is Argentum International, LLC. The 510(k) number is K981299.

When did SILVERLON CONTACT WOUND DRESSING receive FDA 510(k) clearance?

SILVERLON CONTACT WOUND DRESSING received FDA 510(k) clearance on 1998-09-25, under 510(k) number K981299.

Who is the listed applicant for SILVERLON CONTACT WOUND DRESSING?

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

What is the FDA product code for SILVERLON CONTACT WOUND DRESSING?

The FDA product code for SILVERLON CONTACT WOUND DRESSING 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 Argentum International, LLC 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 8 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

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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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