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

EEE

K Number: K953540 · Decision Aug 25, 1995
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
18
Review Days
28

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Basic Information

Device Name
EEE
K Number
K953540
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Edentec Corp.
Date Received
July 28, 1995
Decision Date
August 25, 1995
Product Code
BYD
Advisory Committee
Anesthesiology
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
BYD Condenser, Heat And Moisture (Artificial Nose)

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Other Clearances by Edentec Corp.

K Number Device Name
K953363 OXIFLOW DIGITAL RECORDER
K921819 EDENTEC MODEL 3710 I DIGITAL PRINTER
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)
K891540 EDENTEC MODEL 2860 PRESSURE METER
Search all 18 clearances from Edentec Corp. →