Klock Watch Style Digital Blood Pressure Monitor

FDA 510(k) K023356 · Card Guard Scientific Survival , Ltd.

Substantially Equivalent

510(k) numberK023356

Submission

Device name
Klock Watch Style Digital Blood Pressure Monitor
Applicant
Card Guard Scientific Survival , Ltd.
Rehovot, IL
Received
October 7, 2002
Decision date
January 16, 2003
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.

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Questions and answers

When was Klock Watch Style Digital Blood Pressure Monitor cleared by the FDA?

Klock Watch Style Digital Blood Pressure Monitor (K023356) received a 510(k) decision of Substantially Equivalent on January 16, 2003, 101 days after the submission was received.

What is the product code of K023356?

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