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FDA 510(k)

MeMed BV

K-Number: K222332 · 2023-03-23

ApplicantMeMed Diagnostics, Ltd.
Decision Date2023-03-23
Product CodeQPS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MeMed BV is a medical device manufactured by MeMed Diagnostics, Ltd.. It received FDA 510(k) clearance on 2023-03-23 under approval number K222332. The device is classified under product code QPS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MeMed BV?

MeMed BV is a medical device that received FDA 510(k) clearance on 2023-03-23. It is manufactured by MeMed Diagnostics, Ltd.. The 510(k) number is K222332.

When was MeMed BV approved by the FDA?

MeMed BV received FDA 510(k) clearance on 2023-03-23, under approval number K222332.

What company makes MeMed BV?

MeMed BV is manufactured by MeMed Diagnostics, Ltd..

What is the FDA product code for MeMed BV?

The FDA product code for MeMed BV is QPS.

Other Devices by MeMed Diagnostics, Ltd.

K210254MeMed BV K230944MeMed BV

Related Devices (Code: QPS)

K210254MeMed BVMeMed Diagnostics, Ltd. K213936LIAISON MeMed BV, LIAISON MeMed BV Control SetDiaSorin, Inc. K230944MeMed BVMeMed Diagnostics, Ltd.

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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