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FDA 510(k)

MEDLINE ANTI-REFLUX VALVE

K-Number: K132314 · 2013-09-18

ApplicantMedline Industries, Inc.
Decision Date2013-09-18
Product CodeFEG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDLINE ANTI-REFLUX VALVE 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 2013-09-18 under 510(k) number K132314. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE ANTI-REFLUX VALVE?

MEDLINE ANTI-REFLUX VALVE is a medical device that received FDA 510(k) clearance on 2013-09-18. The listed applicant is Medline Industries, Inc.. The 510(k) number is K132314.

When did MEDLINE ANTI-REFLUX VALVE receive FDA 510(k) clearance?

MEDLINE ANTI-REFLUX VALVE received FDA 510(k) clearance on 2013-09-18, under 510(k) number K132314.

Who is the listed applicant for MEDLINE ANTI-REFLUX VALVE?

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 ANTI-REFLUX VALVE?

The FDA product code for MEDLINE ANTI-REFLUX VALVE is FEG.

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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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