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FDA 510(k) Application Details - K991077
Device Classification Name
Electrode, Depth
More FDA Info for this Device
510(K) Number
K991077
Device Name
Electrode, Depth
Applicant
MICRORECORDING SYSTEMS CONSULTANTS, LLC.
2842 E. FOOTHILL BLVD.
PASADENA, CA 91107 US
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Contact
ROBERT L ROGERS
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Regulation Number
882.1330
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Classification Product Code
GZL
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More FDA Info for this Product Code
Date Received
03/31/1999
Decision Date
06/09/1999
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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