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FDA 510(k) Application Details - K971930
Device Classification Name
Pacemaker Lead Adaptor
More FDA Info for this Device
510(K) Number
K971930
Device Name
Pacemaker Lead Adaptor
Applicant
BIOTRONIK, INC.
6024 JEAN ROAD
LAKE OSWEGO, OR 97035 US
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Contact
KENNETH JENSEN
Other 510(k) Applications for this Contact
Regulation Number
870.3620
More FDA Info for this Regulation Number
Classification Product Code
DTD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/27/1997
Decision Date
08/14/1997
Decision
PT - Substantially Equivalent - Subject to Tracking & PMS
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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