Cleared Traditional

K142932 - Deltex Medical KDP72 Doppler Probe

K142932 is an FDA 510(k) clearance for Deltex Medical KDP72 Doppler Probe, manufactured by Deltex Medical Limited. The device is a Class 2 Cardiovascular device with product code DPT cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K142932 · Deltex Medical Limited · Cardiovascular device
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Jan 2015
Decision
105d
Days
Class 2
Risk

K142932 is an FDA 510(k) clearance for the Deltex Medical KDP72 Doppler Probe. Classified as Probe, Blood-flow, Extravascular (product code DPT), Class II - Special Controls.

Submitted by Deltex Medical Limited (Chichester, West Sussex, GB). The FDA issued a Cleared decision on January 22, 2015 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2120 - 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 Deltex Medical Limited devices

FDA 510(k) Submission Details - K142932

510(k) Number K142932 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 09, 2014
Decision Date January 22, 2015
Days to Decision 105 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
20d faster than avg
Panel avg: 125d · This submission: 105d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DPT Device Classification - Class 2, Special Controls

Product Code DPT Probe, Blood-flow, Extravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2120
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 - DPT Probe, Blood-flow, Extravascular

All 15
Devices cleared under the same product code (DPT) and FDA review panel - the closest regulatory comparables to K142932.
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TRANSTAR PRESSURE TRANSDUCER
K942377 · Medex, Inc. · Aug 1994
TRANSESOPHAGEAL TRANSDUCER THERMAL SAFETY
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