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FDA 510(k)

VASOGRAD DVT COMPRESSION GARMENT

K-Number: K102732 · 2010-10-19

Decision Date2010-10-19
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASOGRAD DVT COMPRESSION GARMENT is the device name listed in this FDA 510(k) record. The listed applicant is Compression Therapy Concepts. It received FDA 510(k) clearance on 2010-10-19 under 510(k) number K102732. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASOGRAD DVT COMPRESSION GARMENT?

VASOGRAD DVT COMPRESSION GARMENT is a medical device that received FDA 510(k) clearance on 2010-10-19. The listed applicant is Compression Therapy Concepts. The 510(k) number is K102732.

When did VASOGRAD DVT COMPRESSION GARMENT receive FDA 510(k) clearance?

VASOGRAD DVT COMPRESSION GARMENT received FDA 510(k) clearance on 2010-10-19, under 510(k) number K102732.

Who is the listed applicant for VASOGRAD DVT COMPRESSION GARMENT?

The FDA 510(k) record lists Compression Therapy Concepts as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASOGRAD DVT COMPRESSION GARMENT?

The FDA product code for VASOGRAD DVT COMPRESSION GARMENT is JOW.

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 Compression Therapy Concepts 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: JOW)

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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