FDA 510(k) Application Details - K781179

Device Classification Name Tools, Pacemaker Service

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510(K) Number K781179
Device Name Tools, Pacemaker Service
Applicant TELECTRONICS, INC.

, US
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Regulation Number 870.3730

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Classification Product Code DTF
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Date Received 07/14/1978
Decision Date 07/27/1978
Decision SE - Substantially Equivalent
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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