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

EDENTEC MODEL 2001 MODULAR MEMORY UNIT (MMU)

K Number: K892227 · Decision Jun 20, 1989
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
18
Review Days
77

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Basic Information

Device Name
EDENTEC MODEL 2001 MODULAR MEMORY UNIT (MMU)
K Number
K892227
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Edentec Corp.
Date Received
April 4, 1989
Decision Date
June 20, 1989
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

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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.
K891540 EDENTEC MODEL 2860 PRESSURE METER
Search all 18 clearances from Edentec Corp. →