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FDA 510(k) Application Details - K012686
Device Classification Name
Electrocardiograph
More FDA Info for this Device
510(K) Number
K012686
Device Name
Electrocardiograph
Applicant
CAIRD TECHNOLOGY
205 CAMDEN CHASE
COLUMBIA, SC 29223 US
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Contact
JAMES H BROWN
Other 510(k) Applications for this Contact
Regulation Number
870.2340
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Classification Product Code
DPS
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More FDA Info for this Product Code
Date Received
08/14/2001
Decision Date
12/13/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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