Cleared Traditional

K020534 - MEDSTAR SYSTEM, MODELS 533-300

K020534 is an FDA 510(k) clearance for MEDSTAR SYSTEM, manufactured by Cybernet Medical. The device is a Class 2 Cardiovascular device with product code DXH cleared through the Traditional 510(k) pathway after a 357-day FDA review.

K020534 · Cybernet Medical · Cardiovascular device
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Optimized for regulatory review, auditing and printing
Feb 2003
Decision
357d
Days
Class 2
Risk

K020534 is an FDA 510(k) clearance for the MEDSTAR SYSTEM, MODELS 533-300. Classified as Transmitters And Receivers, Electrocardiograph, Telephone (product code DXH), Class II - Special Controls.

Submitted by Cybernet Medical (Ann Arbor, US). The FDA issued a Cleared decision on February 11, 2003 after a review of 357 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.2920 - 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. Elevated predicate reliance profile. 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 Cybernet Medical devices

FDA 510(k) Submission Details - K020534

510(k) Number K020534 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 19, 2002
Decision Date February 11, 2003
Days to Decision 357 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
232d slower than avg
Panel avg: 125d · This submission: 357d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXH Device Classification - Class 2, Special Controls

Product Code DXH Transmitters And Receivers, Electrocardiograph, Telephone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2920
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 - DXH Transmitters And Receivers, Electrocardiograph, Telephone

All 168
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