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FDA 510(k)

ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES

K-Number: K060091 · 2006-02-17

ApplicantAlliance Medical Corp.
Decision Date2006-02-17
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES 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 2006-02-17 under 510(k) number K060091. 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 ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES?

ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES is a medical device that received FDA 510(k) clearance on 2006-02-17. The listed applicant is Alliance Medical Corp.. The 510(k) number is K060091.

When did ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES receive FDA 510(k) clearance?

ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES received FDA 510(k) clearance on 2006-02-17, under 510(k) number K060091.

Who is the listed applicant for ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES?

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 ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES?

The FDA product code for ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES is JOW.

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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.

K060648REPROCESSED PHACOEMULSIFICATION TIPSK061045REPROCESSED ELECTROPHYSIOLOGY CATHETERSK060049REPROCESSED COMPRESSION SLEEVESK053316REPROCESSED COMPRESSION SLEEVESK052918REPROCESSED EXTERNAL FIXATION DEVICESK052414REPROCESSED ELECTROPHYSIOLOGY CATHETER

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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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