Cleared Traditional

K142503 - IMED-Z FLUID STATUS MONITOR

K142503 is an FDA 510(k) clearance for IMED-Z FLUID STATUS MONITOR, manufactured by Intersection Medical, Inc.. The device is a Class 2 Cardiovascular device with product code DSB cleared through the Traditional 510(k) pathway after a 273-day FDA review.

K142503 · Intersection Medical, Inc. · Cardiovascular device
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Jun 2015
Decision
273d
Days
Class 2
Risk

K142503 is an FDA 510(k) clearance for the IMED-Z FLUID STATUS MONITOR. Classified as Plethysmograph, Impedance (product code DSB), Class II - Special Controls.

Submitted by Intersection Medical, Inc. (Carlsbad, US). The FDA issued a Cleared decision on June 5, 2015 after a review of 273 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2770 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Intersection Medical, Inc. devices

FDA 510(k) Submission Details - K142503

510(k) Number K142503 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 05, 2014
Decision Date June 05, 2015
Days to Decision 273 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
148d slower than avg
Panel avg: 125d · This submission: 273d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DSB Device Classification - Class 2, Special Controls

Product Code DSB Plethysmograph, Impedance
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2770
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DSB Plethysmograph, Impedance

All 22
Devices cleared under the same product code (DSB) and FDA review panel - the closest regulatory comparables to K142503.
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ECOM ENDOTRACHEAL CARDIAC OUTPUT MONITOR SYSTEM
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BIO Z CARDIO PROFILE HEMODYNAMIC MONITOR
K110645 · Sonosite,Inc. · Jun 2011
C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS
K041434 · Analogic Corp. · Aug 2004