INTERDRY SILVER
K-Number: K110715 · 2011-11-04
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Device Summary
Frequently Asked Questions
What is the INTERDRY SILVER?
INTERDRY SILVER is a medical device that received FDA 510(k) clearance on 2011-11-04. The listed applicant is Milliken Healthcare Products, LLC. The 510(k) number is K110715.
When did INTERDRY SILVER receive FDA 510(k) clearance?
INTERDRY SILVER received FDA 510(k) clearance on 2011-11-04, under 510(k) number K110715.
Who is the listed applicant for INTERDRY SILVER?
The FDA 510(k) record lists Milliken Healthcare Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTERDRY SILVER?
The FDA product code for INTERDRY SILVER is FRL.
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 Milliken Healthcare Products, 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: FRL)
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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