FDA 510(k) Application Details - K830922

Device Classification Name Set, Tubing And Support, Ventilator (W Harness)

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510(K) Number K830922
Device Name Set, Tubing And Support, Ventilator (W Harness)
Applicant CYGNUS RESEARCH CORP.

, US
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Regulation Number 868.5975

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Classification Product Code BZO
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Date Received 03/22/1983
Decision Date 05/02/1983
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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