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FDA 510(k) Application Details - K000690
Device Classification Name
Electrode, Electrocardiograph
More FDA Info for this Device
510(K) Number
K000690
Device Name
Electrode, Electrocardiograph
Applicant
MINNESOTA MINING AND MFG. CO.
3M CENTER
ST. PAUL, MN 55144-1000 US
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Contact
LINDA JOHNSON
Other 510(k) Applications for this Contact
Regulation Number
870.2360
More FDA Info for this Regulation Number
Classification Product Code
DRX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/29/2000
Decision Date
05/17/2000
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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