FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

DG EXAMINER PLUS

K Number: K953799 · Decision Nov 8, 1995
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
53
Applicant Total
8
Review Days
86

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Basic Information

Device Name
DG EXAMINER PLUS
K Number
K953799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medelec , Ltd.
Date Received
August 14, 1995
Decision Date
November 8, 1995
Product Code
OLT
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
OLT Non-Normalizing Quantitative Electroencephalograph Software

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OLT), ordered by most recent decision date.

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Other Clearances by Medelec , Ltd.

K Number Device Name
K965065 TECA. MILLENNIUM
K964280 DG NERVUS
K954157 DG PORTABLE SYSTEM
K953732 TECA PREMIERE
K934670 DG 3P SYSTEM
K934669 ARC
K923303 SAPPHIRE PREMIERE