WIZAIR COMPRESSION SYSTEM
K-Number: K023573 · 2002-11-21
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Device Summary
Frequently Asked Questions
What is the WIZAIR COMPRESSION SYSTEM?
WIZAIR COMPRESSION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-11-21. The listed applicant is Medical Compression Systems (Dbn) , Ltd.. The 510(k) number is K023573.
When did WIZAIR COMPRESSION SYSTEM receive FDA 510(k) clearance?
WIZAIR COMPRESSION SYSTEM received FDA 510(k) clearance on 2002-11-21, under 510(k) number K023573.
Who is the listed applicant for WIZAIR 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 WIZAIR COMPRESSION SYSTEM?
The FDA product code for WIZAIR 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.
Other records listing Medical Compression Systems (Dbn) , Ltd. 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.
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
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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