Medline Single Patient Use Blood Pressure Cuff

FDA 510(k) K071244 · Medline Industries, Inc.

Substantially Equivalent

510(k) numberK071244

Submission

Device name
Medline Single Patient Use Blood Pressure Cuff
Applicant
Medline Industries, Inc.
Mundelein, IL, US
Received
May 3, 2007
Decision date
March 5, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DXQ – Blood Pressure Cuff
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1120
Specialty
Cardiovascular

A blood pressure cuff is a device that has an inflatable bladder in an elastic sleeve (cuff) with a mechanism for inflating the bladder. The cuff is used to determine a subject's blood pressure.

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K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)DXQ · Traditional Baxter Healthcare Corporation12/16/2025SE
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K251045Disposable Neonatal NIBP Cuff (U1682S-C51N); Disposable Neonatal NIBP Cuff…DXQ · Traditional Unimed Medical Supplies, Inc.07/15/2025SE
K242623Disposable Blood Pressure cuff; Reusable Blood Pressure cuffDXQ · Traditional Shenzhen Medke Technology Co., Ltd.10/31/2024SE
K240165Aneroid Sphygmomanometer with Stethoscope; Aneroid SphygmomanometerDXQ · Traditional Wenzhou Longwan Medical Device Factory03/20/2024SE
K233276Reusable Blood Pressure CuffDXQ · Traditional Suzhou Minhua Medical Apparatus Supplies Co., Ltd.12/21/2023SE

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Questions and answers

When was Medline Single Patient Use Blood Pressure Cuff cleared by the FDA?

Medline Single Patient Use Blood Pressure Cuff (K071244) received a 510(k) decision of Substantially Equivalent on March 5, 2008, 307 days after the submission was received.

What is the product code of K071244?

The FDA product code is DXQ – Blood Pressure Cuff, a Class II (moderate risk) device regulated under 21 CFR 870.1120.