FDA 510(k)

MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF

K-Number: K071244 · 2008-03-05

Decision Date2008-03-05

Product CodeDXQ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF 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 2008-03-05 under 510(k) number K071244. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF?

MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 2008-03-05. The listed applicant is Medline Industries, Inc.. The 510(k) number is K071244.

When did MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF receive FDA 510(k) clearance?

MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF received FDA 510(k) clearance on 2008-03-05, under 510(k) number K071244.

Who is the listed applicant for MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF?

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 SINGLE PATIENT USE BLOOD PRESSURE CUFF?

The FDA product code for MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF is DXQ.

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Related Devices (Code: DXQ)

K254287Medline Reusable Blood Pressure CuffMedline Industries, LP K260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffNihon Kohden Corporation K253089NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)Shenzhen Best Electronics Co., Ltd.K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)Unimed Medical Supplies, Inc.K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)Baxter Healthcare Corporation K250765AViTA Arm Type Blood Pressure Monitor CuffAvita Corporation

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.