FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIO-DETEK TRACERITE EEG ELECTRODE

K Number: K920264 · Decision Jun 2, 1992
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
17
Review Days
133

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Basic Information

Device Name
BIO-DETEK TRACERITE EEG ELECTRODE
K Number
K920264
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bio-Detek, Inc.
Date Received
January 21, 1992
Decision Date
June 2, 1992
Product Code
GXY
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
GXY Electrode, Cutaneous

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K071321 POCKETCPR
K040256 PEDI-PADZ RADIOLUCENT MULTI-FUNCTION PEDIATRIC ELECTRODES, MODEL 8900-1005
K040056 BIO-DETEK ELECTRODE ADAPTER, MODEL R2001-90
K033771 BIO-DETEK MODIFIED ADULT MULTI-FUNCTION ELECTRODE WITH CONNECTOR
K984582 ZOLL SUPERPADZ ADULT MULTI-FUNCTION ELECTRODES, MODEL 8900-XXXX
K990106 ZOLL FIRST RESPONDER PADZ ADULT DEFIBRILLATION ELECTRODES
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