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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 the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2019-05-04 under 510(k) 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. The listed applicant is Medline Industries, Inc.. The 510(k) number is K183577.

When did Medline Quick-Clear Wand receive FDA 510(k) clearance?

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

Who is the listed applicant for Medline Quick-Clear Wand?

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 Quick-Clear Wand?

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

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Related Devices (Code: 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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