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FDA 510(k)

COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008

K-Number: K102319 · 2011-01-28

Decision Date2011-01-28
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008 is the device name listed in this FDA 510(k) record. The listed applicant is Won Industrial Co.. It received FDA 510(k) clearance on 2011-01-28 under 510(k) number K102319. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008?

COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008 is a medical device that received FDA 510(k) clearance on 2011-01-28. The listed applicant is Won Industrial Co.. The 510(k) number is K102319.

When did COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008 receive FDA 510(k) clearance?

COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008 received FDA 510(k) clearance on 2011-01-28, under 510(k) number K102319.

Who is the listed applicant for COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008?

The FDA 510(k) record lists Won Industrial Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008?

The FDA product code for COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL WIC-2008 is IRP.

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 Won Industrial Co. 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: IRP)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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