FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Stealth Monitor, Stealth Docking Cable, Stealth DSD Software Installation Disk, Stealth System

K Number: K142468 · Decision Jul 11, 2015
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
3
Review Days
311

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Basic Information

Device Name
Stealth Monitor, Stealth Docking Cable, Stealth DSD Software Installation Disk, Stealth System
K Number
K142468
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiac Insight, Inc.
Date Received
September 3, 2014
Decision Date
July 11, 2015
Product Code
DSH
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DSH Recorder, Magnetic Tape, Medical

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DSH), ordered by most recent decision date.

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Other Clearances by Cardiac Insight, Inc.

K Number Device Name
K162503 Stealth System, Stealth Sensor, Stealth Smart Cable, StealthView Software
K130288 STEALTH MONITOR, STEALTH DOCKING CABLE, STEALTH DISPLAY AND STORAGE DEVICE