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FDA 510(k)

LYMPHA PRESS PLUS DEVICE

K-Number: K013331 · 2001-11-30

ApplicantMego Afek
Decision Date2001-11-30
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LYMPHA PRESS PLUS 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 2001-11-30 under 510(k) number K013331. 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 LYMPHA PRESS PLUS DEVICE?

LYMPHA PRESS PLUS DEVICE is a medical device that received FDA 510(k) clearance on 2001-11-30. The listed applicant is Mego Afek. The 510(k) number is K013331.

When did LYMPHA PRESS PLUS DEVICE receive FDA 510(k) clearance?

LYMPHA PRESS PLUS DEVICE received FDA 510(k) clearance on 2001-11-30, under 510(k) number K013331.

Who is the listed applicant for LYMPHA PRESS PLUS 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 LYMPHA PRESS PLUS DEVICE?

The FDA product code for LYMPHA PRESS PLUS 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 DEVICEK060220PBS MODEL 701A COMPRESSION THERAPY 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

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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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