Cycle BP Monitor and Pulse Oximeter, Model 1060

FDA 510(k) K060820 · Suntech Medical, Inc.

Substantially Equivalent

510(k) numberK060820

Submission

Device name
Cycle BP Monitor and Pulse Oximeter, Model 1060
Applicant
Suntech Medical, Inc.
Morrisville, NC, US
Received
March 27, 2006
Decision date
June 7, 2006
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DXN – System, Measurement, Blood-Pressure, Non-Invasive
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1130
Specialty
Cardiovascular

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Questions and answers

When was Cycle BP Monitor and Pulse Oximeter, Model 1060 cleared by the FDA?

Cycle BP Monitor and Pulse Oximeter, Model 1060 (K060820) received a 510(k) decision of Substantially Equivalent on June 7, 2006, 72 days after the submission was received.

What is the product code of K060820?

The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.