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FDA 510(k)

TORBOT VASCULAR COMPRESSION GARMENTS

K-Number: K061411 · 2006-10-18

Decision Date2006-10-18
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TORBOT VASCULAR COMPRESSION GARMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Torbut Group, Inc.. It received FDA 510(k) clearance on 2006-10-18 under 510(k) number K061411. 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 TORBOT VASCULAR COMPRESSION GARMENTS?

TORBOT VASCULAR COMPRESSION GARMENTS is a medical device that received FDA 510(k) clearance on 2006-10-18. The listed applicant is Torbut Group, Inc.. The 510(k) number is K061411.

When did TORBOT VASCULAR COMPRESSION GARMENTS receive FDA 510(k) clearance?

TORBOT VASCULAR COMPRESSION GARMENTS received FDA 510(k) clearance on 2006-10-18, under 510(k) number K061411.

Who is the listed applicant for TORBOT VASCULAR COMPRESSION GARMENTS?

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

What is the FDA product code for TORBOT VASCULAR COMPRESSION GARMENTS?

The FDA product code for TORBOT VASCULAR COMPRESSION GARMENTS 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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