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

MARS UNITY WORKSTATION WITH HEART RATE VARIABILITY (HRV) OPTION

K Number: K991786 · Decision Nov 18, 1999
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
33
Review Days
177

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Basic Information

Device Name
MARS UNITY WORKSTATION WITH HEART RATE VARIABILITY (HRV) OPTION
K Number
K991786
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
General Electric Medical Systems Information Techn
Date Received
May 25, 1999
Decision Date
November 18, 1999
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by General Electric Medical Systems Information Techn

K Number Device Name
K023380 T-WAVE ALTERMANS (TWA) ALGORITHM OPTION
K021470 SEER LIGHT COMPACT DIGITAL HOLTER RECORDER
K023100 ACCUSKETCH CARDIAC QUANTITATIVE SYSTEM W/ ADVANCED ANALYSIS COMPONENTS
K021454 UNITY NETWORK ID
K020290 DASH 3000/4000 PATIENT MONITOR
K021366 MAC-LAB/CARDIOLAB EP/COMBOLAB
K020661 UNITY IS PATIENT VIEWER
K021325 MODIFICATION OF APEXPRO TELEMETRY SYSTEM
K020524 PATIENTNET MONITORING SYSTEM
K012467 SOLAR 8000M SYSTEM
Search all 33 clearances from General Electric Medical Systems Information Techn →