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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 5 of 5 Results
ProductCode: KPS Applicant: DANISH DIAGNOSTIC DEVELOPMENT A/S Decision Date To: 11/28/2014
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Device Name
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510(K)
Number
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c.cam-ac DANISH DIAGNOSTIC DEVELOPMENT A/S K051460 06/15/2005
cardiomd-ac DANISH DIAGNOSTIC DEVELOPMENT A/S K040616 03/24/2004
c.cam DANISH DIAGNOSTIC DEVELOPMENT A/S K031825 06/20/2003
cardiocam model 9csy0799 DANISH DIAGNOSTIC DEVELOPMENT A/S K011611 06/08/2001
unicorn model sys0630 DANISH DIAGNOSTIC DEVELOPMENT A/S K001888 06/30/2000
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