Decision Date2018-09-20
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Medline Patient Cables and Lead Wires is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2018-09-20 under 510(k) 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. The listed applicant is Medline Industries, Inc.. The 510(k) number is K181726.
When did Medline Patient Cables and Lead Wires receive FDA 510(k) clearance?
Medline Patient Cables and Lead Wires received FDA 510(k) clearance on 2018-09-20, under 510(k) number K181726.
Who is the listed applicant for Medline Patient Cables and Lead Wires?
The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
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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Official Source
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