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

MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701

K Number: K043354 · Decision Jan 10, 2005
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
338
Applicant Total
14
Review Days
35

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Basic Information

Device Name
MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701
K Number
K043354
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Invivo Research, Inc.
Date Received
December 6, 2004
Decision Date
January 10, 2005
Product Code
DRT
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
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

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K974581 MILLENNIA 3500 SERIES MONITOR WITH ANTHESTHETIC AGENT
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K955045 OMNI-TRAK PATIENT MONITORING SYSTEM
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Search all 14 clearances from Invivo Research, Inc. →