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FDA 510(k)

MEDLINE STOPCOCK AND MANIFOLD

K-Number: K120069 · 2012-04-03

ApplicantMedline Industries, Inc.
Decision Date2012-04-03
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDLINE STOPCOCK AND MANIFOLD 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 2012-04-03 under 510(k) number K120069. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE STOPCOCK AND MANIFOLD?

MEDLINE STOPCOCK AND MANIFOLD is a medical device that received FDA 510(k) clearance on 2012-04-03. The listed applicant is Medline Industries, Inc.. The 510(k) number is K120069.

When did MEDLINE STOPCOCK AND MANIFOLD receive FDA 510(k) clearance?

MEDLINE STOPCOCK AND MANIFOLD received FDA 510(k) clearance on 2012-04-03, under 510(k) number K120069.

Who is the listed applicant for MEDLINE STOPCOCK AND MANIFOLD?

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 STOPCOCK AND MANIFOLD?

The FDA product code for MEDLINE STOPCOCK AND MANIFOLD is DTL.

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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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