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FDA 510(k)

MEDLINE BLOOD PRESSURE TRANSDUCER

K-Number: K123095 · 2013-05-08

ApplicantMedline Industries, Inc.
Decision Date2013-05-08
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDLINE BLOOD PRESSURE TRANSDUCER 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 2013-05-08 under 510(k) number K123095. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE BLOOD PRESSURE TRANSDUCER?

MEDLINE BLOOD PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 2013-05-08. The listed applicant is Medline Industries, Inc.. The 510(k) number is K123095.

When did MEDLINE BLOOD PRESSURE TRANSDUCER receive FDA 510(k) clearance?

MEDLINE BLOOD PRESSURE TRANSDUCER received FDA 510(k) clearance on 2013-05-08, under 510(k) number K123095.

Who is the listed applicant for MEDLINE BLOOD PRESSURE TRANSDUCER?

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 BLOOD PRESSURE TRANSDUCER?

The FDA product code for MEDLINE BLOOD PRESSURE TRANSDUCER is DRS.

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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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