DR. SCHOLL'S COMPRESSION SOCKS
K-Number: K123398 · 2012-12-18
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Device Summary
Frequently Asked Questions
What is the DR. SCHOLL'S COMPRESSION SOCKS?
DR. SCHOLL'S COMPRESSION SOCKS is a medical device that received FDA 510(k) clearance on 2012-12-18. The listed applicant is Renfro Corporation. The 510(k) number is K123398.
When did DR. SCHOLL'S COMPRESSION SOCKS receive FDA 510(k) clearance?
DR. SCHOLL'S COMPRESSION SOCKS received FDA 510(k) clearance on 2012-12-18, under 510(k) number K123398.
Who is the listed applicant for DR. SCHOLL'S COMPRESSION SOCKS?
The FDA 510(k) record lists Renfro Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DR. SCHOLL'S COMPRESSION SOCKS?
The FDA product code for DR. SCHOLL'S COMPRESSION SOCKS is DWL.
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.
Related Devices (Code: DWL)
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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