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

ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY)

K Number: K924672 · Decision Dec 15, 1992
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
13
Review Days
90

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Basic Information

Device Name
ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY)
K Number
K924672
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Agilent Technologies
Date Received
September 16, 1992
Decision Date
December 15, 1992
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

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Other Clearances by Agilent Technologies

K Number Device Name
K010949 2010 PLUS HOLTER FOR WINDOWS
K003940 2010 PLUS HOLTER FOR WINDOWS
K003763 2010 PLUS HOLTER FOR WINDOWS
K001308 MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW
K990093 ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW
K980186 ZYMED TELEMETRY SYSTEM
K942781 DIGITAL HOLTER RECORDER
K930806 ZYMED HOLTER SCANNER MODEL 2010
K895208 ZYMED MODEL 1610
K841083 QUIKPAGE ARRHYTHMIA REPORT GENERATOR
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