FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

MEDIPALM-20

K Number: K031202 · Decision May 1, 2003
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
63
Applicant Total
8
Review Days
15

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Basic Information

Device Name
MEDIPALM-20
K Number
K031202
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Braebon Medical Corp.
Date Received
April 16, 2003
Decision Date
May 1, 2003
Product Code
OLV
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OLV Standard Polysomnograph With Electroencephalograph

Similar 510(k) Clearances

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Other Clearances by Braebon Medical Corp.

K Number Device Name
K061764 MEDIBYTE, MODEL MP8
K020312 ULTIMA SNORING MIKE, MODEL 0540
K001743 ULTIMA SMARTBELT, MODEL 0560
K984431 ULTIMA AIRFLOW PRESSURE SENSOR
K981445 ULTIMA AIRFLOW SENSOR, 0510
K982216 ULTIMA RESPIRATORY EFFORT SENSOR MODELS 0520 AND 0522
K981969 ULTIMA BODY POSITION SENSOR