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FDA 510(k) Application Details - K002572
Device Classification Name
Endoscope, Neurological
More FDA Info for this Device
510(K) Number
K002572
Device Name
Endoscope, Neurological
Applicant
MEDTRONIC PS MEDICAL
125 CREMONA DR.
GOLETA, CA 93117-5500 US
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Contact
JANET MCAULEY
Other 510(k) Applications for this Contact
Regulation Number
882.1480
More FDA Info for this Regulation Number
Classification Product Code
GWG
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More FDA Info for this Product Code
Date Received
08/18/2000
Decision Date
11/16/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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