VASOPRESS DVT SYSTEM, MODEL VP500D
K-Number: K061814 · 2006-11-30
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Device Summary
Frequently Asked Questions
What is the VASOPRESS DVT SYSTEM, MODEL VP500D?
VASOPRESS DVT SYSTEM, MODEL VP500D is a medical device that received FDA 510(k) clearance on 2006-11-30. The listed applicant is Compression Therapy Concepts, Inc.. The 510(k) number is K061814.
When did VASOPRESS DVT SYSTEM, MODEL VP500D receive FDA 510(k) clearance?
VASOPRESS DVT SYSTEM, MODEL VP500D received FDA 510(k) clearance on 2006-11-30, under 510(k) number K061814.
Who is the listed applicant for VASOPRESS DVT SYSTEM, MODEL VP500D?
The FDA 510(k) record lists Compression Therapy Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VASOPRESS DVT SYSTEM, MODEL VP500D?
The FDA product code for VASOPRESS DVT SYSTEM, MODEL VP500D 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 Compression Therapy Concepts, Inc. 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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