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FDA 510(k)

PBS MODEL 701A COMPRESSION THERAPY DEVICE

K-Number: K060220 · 2006-02-09

ApplicantMego Afek
Decision Date2006-02-09
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PBS MODEL 701A COMPRESSION THERAPY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Mego Afek. It received FDA 510(k) clearance on 2006-02-09 under 510(k) number K060220. 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 PBS MODEL 701A COMPRESSION THERAPY DEVICE?

PBS MODEL 701A COMPRESSION THERAPY DEVICE is a medical device that received FDA 510(k) clearance on 2006-02-09. The listed applicant is Mego Afek. The 510(k) number is K060220.

When did PBS MODEL 701A COMPRESSION THERAPY DEVICE receive FDA 510(k) clearance?

PBS MODEL 701A COMPRESSION THERAPY DEVICE received FDA 510(k) clearance on 2006-02-09, under 510(k) number K060220.

Who is the listed applicant for PBS MODEL 701A COMPRESSION THERAPY DEVICE?

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

What is the FDA product code for PBS MODEL 701A COMPRESSION THERAPY DEVICE?

The FDA product code for PBS MODEL 701A COMPRESSION THERAPY DEVICE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Mego Afek 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.

K230385Ballancer Platinum (1222)K072372PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICEK013331LYMPHA PRESS PLUS DEVICEK810338LYMPHA PRESS

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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