FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

MICROMED BRAIN SPY PLUS, EMBIA TITANIUM DEVICES

K Number: K071782 · Decision Jan 10, 2008
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
63
Applicant Total
4
Review Days
192

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Basic Information

Device Name
MICROMED BRAIN SPY PLUS, EMBIA TITANIUM DEVICES
K Number
K071782
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micromed S.P.A.
Date Received
July 2, 2007
Decision Date
January 10, 2008
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 Micromed S.P.A.

K Number Device Name
K211974 LED PHOTIC System
K180761 SD LTM STIM Cortical Stimulator
K171384 Micromed BRAIN QUICK system