Cleared Traditional

K060281 - VS-800 VITAL SIGNS MONITOR (FDA 510(k) Clearance)

Jun 2006
Decision
140d
Days
Class 2
Risk

K060281 is an FDA 510(k) clearance for the VS-800 VITAL SIGNS MONITOR. This device is classified as a Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) (Class II - Special Controls, product code MHX).

Submitted by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (Great Neck, US). The FDA issued a Cleared decision on June 23, 2006, 140 days after receiving the submission on February 3, 2006.

This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1025.

Submission Details

510(k) Number K060281 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 03, 2006
Decision Date June 23, 2006
Days to Decision 140 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF

Device Classification

Product Code MHX — Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)
Device Class Class II - Special Controls
CFR Regulation 21 CFR 870.1025

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