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FDA 510(k)

COMPRESSIBLE LIMB SLEEVE

K-Number: K011192 · 2001-11-26

Decision Date2001-11-26
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COMPRESSIBLE LIMB SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Medical Corp.. It received FDA 510(k) clearance on 2001-11-26 under 510(k) number K011192. 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 COMPRESSIBLE LIMB SLEEVE?

COMPRESSIBLE LIMB SLEEVE is a medical device that received FDA 510(k) clearance on 2001-11-26. The listed applicant is Alliance Medical Corp.. The 510(k) number is K011192.

When did COMPRESSIBLE LIMB SLEEVE receive FDA 510(k) clearance?

COMPRESSIBLE LIMB SLEEVE received FDA 510(k) clearance on 2001-11-26, under 510(k) number K011192.

Who is the listed applicant for COMPRESSIBLE LIMB SLEEVE?

The FDA 510(k) record lists Alliance Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPRESSIBLE LIMB SLEEVE?

The FDA product code for COMPRESSIBLE LIMB SLEEVE 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 Alliance Medical Corp. 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 36 devices →

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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