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FDA 510(k)

REPROCESSED COMPRESSION SLEEVE

K-Number: K021654 · 2003-02-05

ApplicantAlliance Medical, Inc.
Decision Date2003-02-05
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REPROCESSED COMPRESSION SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Medical, Inc.. It received FDA 510(k) clearance on 2003-02-05 under 510(k) number K021654. 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 REPROCESSED COMPRESSION SLEEVE?

REPROCESSED COMPRESSION SLEEVE is a medical device that received FDA 510(k) clearance on 2003-02-05. The listed applicant is Alliance Medical, Inc.. The 510(k) number is K021654.

When did REPROCESSED COMPRESSION SLEEVE receive FDA 510(k) clearance?

REPROCESSED COMPRESSION SLEEVE received FDA 510(k) clearance on 2003-02-05, under 510(k) number K021654.

Who is the listed applicant for REPROCESSED COMPRESSION SLEEVE?

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

What is the FDA product code for REPROCESSED COMPRESSION SLEEVE?

The FDA product code for REPROCESSED COMPRESSION SLEEVE is JOW.

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Other records listing Alliance Medical, 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.

K051438VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM)K050518REPROCESSED PHACOEMUISIFICATION TIPSK030187REPROCESSED ELECTROPHYSIOLOGY CATHETERK012634REPROCESSED EXTERNAL FIXATION DEVICEK012630REPROCESSED LINVATEC ARTHROSCOPIC BURSK012613REPROCSSED LINVATEC SHAVERS

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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.

K261807Sequential Circulator (SC-4004-DL, SC-4008-DL)Bio Compression Systems, Inc.K254217AerloomEvolym, LLCK253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile MedicalK253386DVT GarmentVistar Medical Supplies Co., Ltd.K250242Compression Therapy Device (LGT-2202DVT)Guangzhou Longest Medical Technology Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , Ltd.

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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