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FDA 510(k)

VASOPRESS SUPREME MINI MODEL VP500DM

K-Number: K101915 · 2010-08-06

Decision Date2010-08-06
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASOPRESS SUPREME MINI MODEL VP500DM is the device name listed in this FDA 510(k) record. The listed applicant is Compression Therapy Concepts, Inc.. It received FDA 510(k) clearance on 2010-08-06 under 510(k) number K101915. 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 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

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