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

ESCORT LINK CENTRAL STATION MONITOR

K Number: K970012 · Decision Jun 26, 1997
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
27
Review Days
175

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Basic Information

Device Name
ESCORT LINK CENTRAL STATION MONITOR
K Number
K970012
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medical Data Electronics
Date Received
January 2, 1997
Decision Date
June 26, 1997
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

Similar 510(k) Clearances

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

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Other Clearances by Medical Data Electronics

K Number Device Name
K014294 MODIFICATION TO ESCORT II+ 400 SERIES 9ESCORT PRISM) MONITOR, MODELS 20400, 20401, 20403, 20411, 20412, 20413, 20414
K012336 MODIFICATION TO:ESCORT VISION CENTRAL STATION TELEMETRY SYSTEM, MODEL 20500
K000660 ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413
K992413 ESCORT 100/300 SERIES B (ESCORT II) PATIENT MONITOR
K992411 ESCORT II+ 400 SERIES (ESCORT PRISM) MONITOR
K982104 ESCORT-LINK CENTRAL STATION MONITOR MODEL 20500
K970763 MODULAR TELEMETRY SYSTEM (MTS) OPTION FOR THE MDE ESCORT II MONITOR
K970011 ESCORT II CLINICAL THERMOMETRY MODULE (CTM)
K961138 ESORT II + 400 SERIES MONITOR
K943256 CARDIAC OUTPUT OPTION 39
Search all 27 clearances from Medical Data Electronics →