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FDA 510(k)

Medline Patient Cables and Lead Wires

K-Number: K181726 · 2018-09-20

ApplicantMedline Industries, Inc.
Decision Date2018-09-20
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Medline Patient Cables and Lead Wires is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2018-09-20 under approval number K181726. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline Patient Cables and Lead Wires?

Medline Patient Cables and Lead Wires is a medical device that received FDA 510(k) clearance on 2018-09-20. It is manufactured by Medline Industries, Inc.. The 510(k) number is K181726.

When was Medline Patient Cables and Lead Wires approved by the FDA?

Medline Patient Cables and Lead Wires received FDA 510(k) clearance on 2018-09-20, under approval number K181726.

What company makes Medline Patient Cables and Lead Wires?

Medline Patient Cables and Lead Wires is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Patient Cables and Lead Wires?

The FDA product code for Medline Patient Cables and Lead Wires is DSA.

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Related Devices (Code: DSA)

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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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