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FDA 510(k) Application Details - K020910
Device Classification Name
Electrode, Needle
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510(K) Number
K020910
Device Name
Electrode, Needle
Applicant
THE ELECTRODE STORE, INC.
936-11TH AVENUE EAST
SEATTLE, WA 98102 US
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Contact
CARL YOUNGMANN
Other 510(k) Applications for this Contact
Regulation Number
882.1350
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Classification Product Code
GXZ
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More FDA Info for this Product Code
Date Received
03/20/2002
Decision Date
07/19/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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