VASOPRESS SUPREME MINI MODEL VP500DM
K-Number: K101915 · 2010-08-06
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Device Summary
Frequently Asked Questions
What is the VASOPRESS SUPREME MINI MODEL VP500DM?
VASOPRESS SUPREME MINI MODEL VP500DM is a medical device that received FDA 510(k) clearance on 2010-08-06. The listed applicant is Compression Therapy Concepts, Inc.. The 510(k) number is K101915.
When did VASOPRESS SUPREME MINI MODEL VP500DM receive FDA 510(k) clearance?
VASOPRESS SUPREME MINI MODEL VP500DM received FDA 510(k) clearance on 2010-08-06, under 510(k) number K101915.
Who is the listed applicant for VASOPRESS SUPREME MINI MODEL VP500DM?
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 SUPREME MINI MODEL VP500DM?
The FDA product code for VASOPRESS SUPREME MINI MODEL VP500DM 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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