FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

EDENTEC MODEL 4700 SCANNER

K Number: K884388 · Decision Jan 10, 1989
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
86
Applicant Total
18
Review Days
84

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Basic Information

Device Name
EDENTEC MODEL 4700 SCANNER
K Number
K884388
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.2810
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Edentec Corp.
Date Received
October 18, 1988
Decision Date
January 10, 1989
Product Code
DSF
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
DSF Recorder, Paper Chart

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K Number Device Name
K953363 OXIFLOW DIGITAL RECORDER
K953540 EEE
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K913749 EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170
K910871 EDENTEC DIGITAL CHARTER MODEL 3710
K910870 EDENTEC MODEL 3711 DIGITAL RECORDER
K905575 MODIFIED MODELS 2000W AND 2000W OPTION H APNEA MON
K901060 EDENTEC MODEL 2000W SYSTEM 700 MONITOR
K893561 EDENTRACE 670 SYSTEM MULTICHANNEL RECORDER W/OXIM.
K892227 EDENTEC MODEL 2001 MODULAR MEMORY UNIT (MMU)
Search all 18 clearances from Edentec Corp. →