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

ESCORT PULSE OXIMETRY OPTION

K Number: K892120 · Decision Sep 26, 1989
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
27
Review Days
179

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Basic Information

Device Name
ESCORT PULSE OXIMETRY OPTION
K Number
K892120
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Medical Data Electronics
Date Received
March 31, 1989
Decision Date
September 26, 1989
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
DQA Oximeter

Similar 510(k) Clearances

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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)
K970012 ESCORT LINK CENTRAL STATION MONITOR
K961138 ESORT II + 400 SERIES MONITOR
Search all 27 clearances from Medical Data Electronics →