Genericuff

FDA 510(k) K953466 · Generic Medical, Inc.

Substantially Equivalent

510(k) numberK953466

Submission

Device name
Genericuff
Applicant
Generic Medical, Inc.
Alpharetta, GA, US
Received
July 24, 1995
Decision date
September 15, 1995
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.

Other 510(k)s with product code DXQ

510(k)DeviceApplicantDecision
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

Questions and answers

When was Genericuff cleared by the FDA?

Genericuff (K953466) received a 510(k) decision of Substantially Equivalent on September 15, 1995, 53 days after the submission was received.

What is the product code of K953466?

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