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FDA 510(k)

PROAIR 3000 COMPRESSION SYSTEM

K-Number: K993758 · 2000-05-19

ApplicantMedical Compression Systems (Dbn) , Ltd.
Decision Date2000-05-19
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PROAIR 3000 COMPRESSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Compression Systems (Dbn) , Ltd.. It received FDA 510(k) clearance on 2000-05-19 under 510(k) number K993758. 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 PROAIR 3000 COMPRESSION SYSTEM?

PROAIR 3000 COMPRESSION SYSTEM is a medical device that received FDA 510(k) clearance on 2000-05-19. The listed applicant is Medical Compression Systems (Dbn) , Ltd.. The 510(k) number is K993758.

When did PROAIR 3000 COMPRESSION SYSTEM receive FDA 510(k) clearance?

PROAIR 3000 COMPRESSION SYSTEM received FDA 510(k) clearance on 2000-05-19, under 510(k) number K993758.

Who is the listed applicant for PROAIR 3000 COMPRESSION SYSTEM?

The FDA 510(k) record lists Medical Compression Systems (Dbn) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROAIR 3000 COMPRESSION SYSTEM?

The FDA product code for PROAIR 3000 COMPRESSION SYSTEM is JOW.

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Other records listing Medical Compression Systems (Dbn) , Ltd. as applicant

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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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