FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

MODEL 4000 EVOKED POTENTIAL MEASUREMENT SYSTEM

K Number: K894608 · Decision Dec 29, 1989
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
5
Review Days
164

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Basic Information

Device Name
MODEL 4000 EVOKED POTENTIAL MEASUREMENT SYSTEM
K Number
K894608
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Micro-Shev , Ltd.
Date Received
July 18, 1989
Decision Date
December 29, 1989
Product Code
GWF
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
GWF Stimulator, Electrical, Evoked Response

Similar 510(k) Clearances

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

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Other Clearances by Micro-Shev , Ltd.

K Number Device Name
K913785 CORONET 100
K900378 EMG OPTION FOR MICROSHEV 4000
K874193 MICROSHEV MODEL 2000
K792085 C-ERA-100 COMPUTERIZED ELECTRIC RESPON