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FDA 510(k)

Medline Hemo-Force DVT Compression Sleeve

K-Number: K170415 · 2017-09-08

ApplicantMedline Industries, Inc.
Decision Date2017-09-08
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Medline Hemo-Force DVT Compression Sleeve is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2017-09-08 under approval number K170415. 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 Medline Hemo-Force DVT Compression Sleeve?

Medline Hemo-Force DVT Compression Sleeve is a medical device that received FDA 510(k) clearance on 2017-09-08. It is manufactured by Medline Industries, Inc.. The 510(k) number is K170415.

When was Medline Hemo-Force DVT Compression Sleeve approved by the FDA?

Medline Hemo-Force DVT Compression Sleeve received FDA 510(k) clearance on 2017-09-08, under approval number K170415.

What company makes Medline Hemo-Force DVT Compression Sleeve?

Medline Hemo-Force DVT Compression Sleeve is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Hemo-Force DVT Compression Sleeve?

The FDA product code for Medline Hemo-Force DVT Compression Sleeve is JOW.

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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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