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FDA 510(k)

TRAVELAIR PORTABLE COMPRESSION SYSTEM

K-Number: K022340 · 2003-02-19

Decision Date2003-02-19
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRAVELAIR PORTABLE COMPRESSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dynamic Air, Inc.. It received FDA 510(k) clearance on 2003-02-19 under 510(k) number K022340. 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 TRAVELAIR PORTABLE COMPRESSION SYSTEM?

TRAVELAIR PORTABLE COMPRESSION SYSTEM is a medical device that received FDA 510(k) clearance on 2003-02-19. The listed applicant is Dynamic Air, Inc.. The 510(k) number is K022340.

When did TRAVELAIR PORTABLE COMPRESSION SYSTEM receive FDA 510(k) clearance?

TRAVELAIR PORTABLE COMPRESSION SYSTEM received FDA 510(k) clearance on 2003-02-19, under 510(k) number K022340.

Who is the listed applicant for TRAVELAIR PORTABLE COMPRESSION SYSTEM?

The FDA 510(k) record lists Dynamic Air, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRAVELAIR PORTABLE COMPRESSION SYSTEM?

The FDA product code for TRAVELAIR PORTABLE COMPRESSION SYSTEM 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.

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.

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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