FDA 510(k) Application Details - K841817

Device Classification Name System, Imaging, Pulsed Echo, Ultrasonic

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510(K) Number K841817
Device Name System, Imaging, Pulsed Echo, Ultrasonic
Applicant TECHNICARE CORP.


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Regulation Number 892.1560

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Classification Product Code IYO
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Date Received 05/01/1984
Decision Date 08/17/1984
Decision SE - Substantially Equivalent
Classification Advisory Committee OB - Obstetrics/Gynecology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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