Neonatal/Sterile/Dispos/Noninvas Blood Press Cuff

FDA 510(k) K905101 · Hewlett-Packard Co.

Substantially Equivalent

510(k) numberK905101

Submission

Device name
Neonatal/Sterile/Dispos/Noninvas Blood Press Cuff
Applicant
Hewlett-Packard Co.
Andover, MA, US
Received
November 13, 1990
Decision date
December 20, 1990
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.

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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

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Questions and answers

When was Neonatal/Sterile/Dispos/Noninvas Blood Press Cuff cleared by the FDA?

Neonatal/Sterile/Dispos/Noninvas Blood Press Cuff (K905101) received a 510(k) decision of Substantially Equivalent on December 20, 1990, 37 days after the submission was received.

What is the product code of K905101?

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