Imed-Z Fluid Status Monitor

FDA 510(k) K142503 · Intersection Medical, Inc.

Substantially Equivalent

510(k) numberK142503

Submission

Device name
Imed-Z Fluid Status Monitor
Applicant
Intersection Medical, Inc.
Carlsbad, CA, US
Received
September 5, 2014
Decision date
June 5, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DSB – Plethysmograph, Impedance
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2770
Specialty
Cardiovascular

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Questions and answers

When was Imed-Z Fluid Status Monitor cleared by the FDA?

Imed-Z Fluid Status Monitor (K142503) received a 510(k) decision of Substantially Equivalent on June 5, 2015, 273 days after the submission was received.

What is the product code of K142503?

The FDA product code is DSB – Plethysmograph, Impedance, a Class II (moderate risk) device regulated under 21 CFR 870.2770.