Cleared Traditional

K102968 - INFINITY CNAP SMARTPOD (FDA 510(k) Clearance)

Feb 2011
Decision
135d
Days
Class 2
Risk

K102968 is an FDA 510(k) clearance for the INFINITY CNAP SMARTPOD. This device is classified as a System, Measurement, Blood-pressure, Non-invasive (Class II - Special Controls, product code DXN).

Submitted by Draeger Medical Systems, Inc. (Andover, US). The FDA issued a Cleared decision on February 18, 2011, 135 days after receiving the submission on October 6, 2010.

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

Submission Details

510(k) Number K102968 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 06, 2010
Decision Date February 18, 2011
Days to Decision 135 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF

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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