Cleared Traditional

K130594 - ENSITE VELOCITY SYSTEM

K130594 is an FDA 510(k) clearance for ENSITE VELOCITY SYSTEM, manufactured by St Jude Medical. The device is a Class 2 Cardiovascular device with product code DQK cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K130594 · St Jude Medical · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2013
Decision
57d
Days
Class 2
Risk

K130594 is an FDA 510(k) clearance for the ENSITE VELOCITY SYSTEM. Classified as Computer, Diagnostic, Programmable (product code DQK), Class II - Special Controls.

Submitted by St Jude Medical (St. Paul, US). The FDA issued a Cleared decision on May 3, 2013 after a review of 57 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1425 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all St Jude Medical devices

FDA 510(k) Submission Details - K130594

510(k) Number K130594 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 2013
Decision Date May 03, 2013
Days to Decision 57 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 125d · This submission: 57d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQK Device Classification - Class 2, Special Controls

Product Code DQK Computer, Diagnostic, Programmable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1425
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 - DQK Computer, Diagnostic, Programmable

All 373
Devices cleared under the same product code (DQK) and FDA review panel - the closest regulatory comparables to K130594.
SENSIS, SENSIS LITE
K131812 · Siemens Medi Cal Solutions, Inc. · Jul 2013
RHYTHMIA MAPPING SYSTEM
K130750 · Rhythmia Medical, Inc. · Jul 2013
ENTERPRISE ECG ANALYSIS / INTERPRETATION SOFTWARE
K131045 · Cardiac Designs, LLC · May 2013
MAC-LAB HEMODYNAMIC RECORDING SYSTEM
K130626 · Ge Medical Systems Information Technologies, Inc. · May 2013
RHYTHM VIEW
K123295 · Topera, Inc. · Apr 2013
QUANTIEN MEASUREMENT SYSTEM
K123984 · Radi Medical Systems AB · Mar 2013