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FDA 510(k)

Medline Quick-Clear Wand

K-Number: K183577 · 2019-05-04

ApplicantMedline Industries, Inc.
Decision Date2019-05-04
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Medline Quick-Clear Wand is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2019-05-04 under approval number K183577. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline Quick-Clear Wand?

Medline Quick-Clear Wand is a medical device that received FDA 510(k) clearance on 2019-05-04. It is manufactured by Medline Industries, Inc.. The 510(k) number is K183577.

When was Medline Quick-Clear Wand approved by the FDA?

Medline Quick-Clear Wand received FDA 510(k) clearance on 2019-05-04, under approval number K183577.

What company makes Medline Quick-Clear Wand?

Medline Quick-Clear Wand is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Quick-Clear Wand?

The FDA product code for Medline Quick-Clear Wand is KNT.

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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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