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FDA 510(k)

MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS

K-Number: K101702 · 2010-08-27

ApplicantMidwest Reprocessing Center, LLC
Decision Date2010-08-27
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Reprocessing Center, LLC. It received FDA 510(k) clearance on 2010-08-27 under 510(k) number K101702. 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 MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS?

MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS is a medical device that received FDA 510(k) clearance on 2010-08-27. The listed applicant is Midwest Reprocessing Center, LLC. The 510(k) number is K101702.

When did MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS receive FDA 510(k) clearance?

MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS received FDA 510(k) clearance on 2010-08-27, under 510(k) number K101702.

Who is the listed applicant for MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS?

The FDA 510(k) record lists Midwest Reprocessing Center, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS?

The FDA product code for MIDWEST REPROCESSING CENTER REPROCESSED VENODYNE SLEEVES/FOOT CUFFS is JOW.

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Other records listing Midwest Reprocessing Center, LLC 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.

K111007MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST REK101280MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBEK101330MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE

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

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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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