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FDA 510(k)

MedHealth DVT compression Devices MHH900S/MHH900E

K-Number: K231801 · 2023-12-14

ApplicantMedhealth Medical Limited
Decision Date2023-12-14
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MedHealth DVT compression Devices MHH900S/MHH900E is a medical device manufactured by Medhealth Medical Limited. It received FDA 510(k) clearance on 2023-12-14 under approval number K231801. 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 MedHealth DVT compression Devices MHH900S/MHH900E?

MedHealth DVT compression Devices MHH900S/MHH900E is a medical device that received FDA 510(k) clearance on 2023-12-14. It is manufactured by Medhealth Medical Limited. The 510(k) number is K231801.

When was MedHealth DVT compression Devices MHH900S/MHH900E approved by the FDA?

MedHealth DVT compression Devices MHH900S/MHH900E received FDA 510(k) clearance on 2023-12-14, under approval number K231801.

What company makes MedHealth DVT compression Devices MHH900S/MHH900E?

MedHealth DVT compression Devices MHH900S/MHH900E is manufactured by Medhealth Medical Limited.

What is the FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E?

The FDA product code for MedHealth DVT compression Devices MHH900S/MHH900E is JOW.

Related Clinical Trials

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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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