SILVERLON WOUND PACKING STRIPS
K-Number: K984210 · 1999-09-24
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Device Summary
Frequently Asked Questions
What is the SILVERLON WOUND PACKING STRIPS?
SILVERLON WOUND PACKING STRIPS is a medical device that received FDA 510(k) clearance on 1999-09-24. The listed applicant is Argentum International, LLC. The 510(k) number is K984210.
When did SILVERLON WOUND PACKING STRIPS receive FDA 510(k) clearance?
SILVERLON WOUND PACKING STRIPS received FDA 510(k) clearance on 1999-09-24, under 510(k) number K984210.
Who is the listed applicant for SILVERLON WOUND PACKING STRIPS?
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 WOUND PACKING STRIPS?
The FDA product code for SILVERLON WOUND PACKING STRIPS 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.
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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