Aneroid Sphygmomanometer with Stethoscope Model Hbpk-A

FDA 510(k) K082542 · Cardicare Company, Ltd.

Substantially Equivalent

510(k) numberK082542

Submission

Device name
Aneroid Sphygmomanometer with Stethoscope Model Hbpk-A
Applicant
Cardicare Company, Ltd.
Hangzhou, Zhejiang, CN
Received
September 3, 2008
Decision date
September 17, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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

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K222652Aneroid Sphygmomanometer; Single Patient Use Aneroid SphygmomanometerDXQ · Traditional 11/28/2022SE

Questions and answers

When was Aneroid Sphygmomanometer with Stethoscope Model Hbpk-A cleared by the FDA?

Aneroid Sphygmomanometer with Stethoscope Model Hbpk-A (K082542) received a 510(k) decision of Substantially Equivalent on September 17, 2008, 14 days after the submission was received.

What is the product code of K082542?

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