Cleared Special

K050711 - FULL AUTOMATIC (NIBP) BLOOD PRESSURE MONITOR, MODEL HL168JT (FDA 510(k) Clearance)

Apr 2005
Decision
20d
Days
Class 2
Risk

K050711 is an FDA 510(k) clearance for the FULL AUTOMATIC (NIBP) BLOOD PRESSURE MONITOR, MODEL HL168JT. This device is classified as a System, Measurement, Blood-pressure, Non-invasive (Class II - Special Controls, product code DXN).

Submitted by Health & Life Co., Ltd. (Chung Ho City, Taipei, Hsien, TW). The FDA issued a Cleared decision on April 7, 2005, 20 days after receiving the submission on March 18, 2005.

This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1130.

Submission Details

510(k) Number K050711 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 18, 2005
Decision Date April 07, 2005
Days to Decision 20 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Statement

Device Classification

Product Code DXN — System, Measurement, Blood-pressure, Non-invasive
Device Class Class II - Special Controls
CFR Regulation 21 CFR 870.1130

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