FDA 510(k) Application Details - K822590

Device Classification Name System, Signal Isolation

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510(K) Number K822590
Device Name System, Signal Isolation
Applicant HONEYWELL, INC.

, US
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Regulation Number 870.2600

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Classification Product Code DRJ
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Date Received 09/07/1982
Decision Date 10/04/1982
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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