Cleared Abbreviated

K113183 - PMS8210A (IRIS) MULTI-PARAMETER PATIENT MONITOR, MODEL CODE 500

K113183 is an FDA 510(k) clearance for PMS8210A (IRIS) MULTI-PARAMETER PATIENT..., manufactured by Shanghai 3f Electronics Co, Ltd.. The device is a Class 2 Cardiovascular device with product code MWI cleared through the Abbreviated 510(k) pathway after a 104-day FDA review.

K113183 · Shanghai 3f Electronics Co, Ltd. · Cardiovascular device
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Optimized for regulatory review, auditing and printing
Feb 2012
Decision
104d
Days
Class 2
Risk

K113183 is an FDA 510(k) clearance for the PMS8210A (IRIS) MULTI-PARAMETER PATIENT MONITOR, MODEL CODE 500. Classified as Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms) (product code MWI), Class II - Special Controls.

Submitted by Shanghai 3f Electronics Co, Ltd. (Echo, US). The FDA issued a Cleared decision on February 9, 2012 after a review of 104 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2300 - the FDA cardiovascular device oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Shanghai 3f Electronics Co, Ltd. devices

FDA 510(k) Submission Details - K113183

510(k) Number K113183 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 2011
Decision Date February 09, 2012
Days to Decision 104 days
Submission Type Abbreviated
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
21d faster than avg
Panel avg: 125d · This submission: 104d
Pathway characteristics
Standards-based clearance path.

MWI Device Classification - Class 2, Special Controls

Product Code MWI Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2300
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 - MWI Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms)

All 176
Devices cleared under the same product code (MWI) and FDA review panel - the closest regulatory comparables to K113183.
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