Rossmax Digital Sphygmomanometer Mandaus II

FDA 510(k) K053006 · Rossmax Internationl , Ltd.

Substantially Equivalent

510(k) numberK053006

Submission

Device name
Rossmax Digital Sphygmomanometer Mandaus II
Applicant
Rossmax Internationl , Ltd.
Taipei, TW
Received
October 26, 2005
Decision date
February 3, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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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K020897Rossmax Automatic Wrist Blood Pressure Monitor, Models B150 & Q400DXN · Abbreviated 08/06/2002SE
K010498Wristwatch Blood Pressure Monitor A46DXN · Special 03/20/2001SE
K010190Wristwatch Blood Pressure Monitor, Model A43DXN · Special 02/08/2001SE

Questions and answers

When was Rossmax Digital Sphygmomanometer Mandaus II cleared by the FDA?

Rossmax Digital Sphygmomanometer Mandaus II (K053006) received a 510(k) decision of Substantially Equivalent on February 3, 2006, 100 days after the submission was received.

What is the product code of K053006?

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