Blood Pressure Cuff

FDA 510(k) K881799 · Biomedical Dynamics, Inc.

Substantially Equivalent

510(k) numberK881799

Submission

Device name
Blood Pressure Cuff
Applicant
Biomedical Dynamics, Inc.
Minneapolis, MN, US
Received
April 27, 1988
Decision date
October 14, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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.

Other 510(k)s with product code DXQ

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K254287Medline Reusable Blood Pressure CuffDXQ · Traditional Medline Industries, LP06/22/2026SE
K260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffDXQ · Traditional Nihon Kohden Corporation05/06/2026SE
K253089NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122…DXQ · Traditional Shenzhen Best Electronics Co., Ltd.02/13/2026SE
K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)DXQ · Special Unimed Medical Supplies, Inc.01/09/2026SE
K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)DXQ · Traditional Baxter Healthcare Corporation12/16/2025SE
K250765AViTA Arm Type Blood Pressure Monitor CuffDXQ · Traditional Avita Corporation09/03/2025SE
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

More from Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

510(k)DeviceDecision
K915074Irrigator/Aspirator ProbeHMX · Traditional 02/05/1992SE
K913751Pressure InfuserKZD · Traditional 01/09/1992SE
K911213CuffableDXQ · Traditional 08/07/1991SE
K911216InfusableKZD · Traditional 07/22/1991SE
K911324Irrigation/Aspiration Tubing SetKDH · Traditional 06/24/1991SE
K904376Aneroid Blood Pressure GaugeFCY · Traditional 12/20/1990SE
K890268Pressure Infusor for I.V. Bags/AutoinflationKPE · Traditional 05/05/1989SE
K861977Biomedical Dynamics Disposable Pressure InfusorKZD · Traditional 07/15/1986SE
K850506Correct Flo Intravascular Administration SetFPA · Traditional 04/01/1985SE

Questions and answers

When was Blood Pressure Cuff cleared by the FDA?

Blood Pressure Cuff (K881799) received a 510(k) decision of Substantially Equivalent on October 14, 1988, 170 days after the submission was received.

What is the product code of K881799?

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