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FDA 510(k)

DR. SCHOLL'S COMPRESSION SOCKS

K-Number: K123398 · 2012-12-18

Decision Date2012-12-18
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DR. SCHOLL'S COMPRESSION SOCKS is the device name listed in this FDA 510(k) record. The listed applicant is Renfro Corporation. It received FDA 510(k) clearance on 2012-12-18 under 510(k) number K123398. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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