Tytan Blood Pressure Cuff

FDA 510(k) K062238 · Tytan Medical Corp.

Substantially Equivalent

510(k) numberK062238

Submission

Device name
Tytan Blood Pressure Cuff
Applicant
Tytan Medical Corp.
Hsin-Chu City, TW
Received
August 2, 2006
Decision date
September 21, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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.

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

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K092893Tytan Automatic Aneroid Sphygmomanometer, Model A730 and Manual Digital LCD…DXN · Traditional 01/14/2010SE
K033025Tytan Professional /Economy Series Sphygmomanometer, No 710/NO 700DXN · Traditional 12/10/2003SE
K023637Tytan Electronic Stethoscopes (Model #600)DQD · Traditional 02/26/2003SE

Questions and answers

When was Tytan Blood Pressure Cuff cleared by the FDA?

Tytan Blood Pressure Cuff (K062238) received a 510(k) decision of Substantially Equivalent on September 21, 2006, 50 days after the submission was received.

What is the product code of K062238?

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