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FDA 510(k)

CURAD COMPRESSION HOSIERY

K-Number: K112769 · 2012-03-01

Decision Date2012-03-01
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CURAD COMPRESSION HOSIERY is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2012-03-01 under 510(k) number K112769. 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 CURAD COMPRESSION HOSIERY?

CURAD COMPRESSION HOSIERY is a medical device that received FDA 510(k) clearance on 2012-03-01. The listed applicant is Medline Industries, Inc.. The 510(k) number is K112769.

When did CURAD COMPRESSION HOSIERY receive FDA 510(k) clearance?

CURAD COMPRESSION HOSIERY received FDA 510(k) clearance on 2012-03-01, under 510(k) number K112769.

Who is the listed applicant for CURAD COMPRESSION HOSIERY?

The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURAD COMPRESSION HOSIERY?

The FDA product code for CURAD COMPRESSION HOSIERY 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.

Other records listing Medline Industries, Inc. 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 223 devices →

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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