Cleared Traditional

K102111 - MEDICAL MAGNETIC TAPE RECORDER

K102111 is an FDA 510(k) clearance for MEDICAL MAGNETIC TAPE RECORDER, manufactured by Wpr Medical AS. The device is a Class 2 Cardiovascular device with product code DSI cleared through the Traditional 510(k) pathway after a 132-day FDA review.

K102111 · Wpr Medical AS · Cardiovascular device
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Dec 2010
Decision
132d
Days
Class 2
Risk

K102111 is an FDA 510(k) clearance for the MEDICAL MAGNETIC TAPE RECORDER. Classified as Detector And Alarm, Arrhythmia (product code DSI), Class II - Special Controls.

Submitted by Wpr Medical AS (Ne, US). The FDA issued a Cleared decision on December 7, 2010 after a review of 132 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1025 - 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 Wpr Medical AS devices

FDA 510(k) Submission Details - K102111

510(k) Number K102111 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 2010
Decision Date December 07, 2010
Days to Decision 132 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
7d slower than avg
Panel avg: 125d · This submission: 132d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DSI Device Classification - Class 2, Special Controls

Product Code DSI Detector And Alarm, Arrhythmia
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1025
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 - DSI Detector And Alarm, Arrhythmia

All 271
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