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FDA 510(k)

ACTIVECARE DVT ACTIVECARE+SFT

K-Number: K113525 · 2012-01-31

Decision Date2012-01-31
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACTIVECARE DVT ACTIVECARE+SFT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Compression Systems (Dbn) , Ltd.. It received FDA 510(k) clearance on 2012-01-31 under 510(k) number K113525. 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 ACTIVECARE DVT ACTIVECARE+SFT?

ACTIVECARE DVT ACTIVECARE+SFT is a medical device that received FDA 510(k) clearance on 2012-01-31. The listed applicant is Medical Compression Systems (Dbn) , Ltd.. The 510(k) number is K113525.

When did ACTIVECARE DVT ACTIVECARE+SFT receive FDA 510(k) clearance?

ACTIVECARE DVT ACTIVECARE+SFT received FDA 510(k) clearance on 2012-01-31, under 510(k) number K113525.

Who is the listed applicant for ACTIVECARE DVT ACTIVECARE+SFT?

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 ACTIVECARE DVT ACTIVECARE+SFT?

The FDA product code for ACTIVECARE DVT ACTIVECARE+SFT 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.

View all 9 devices →

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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