FDA 510(k) Application Details - K802659

Device Classification Name Flowmeter, Tube, Thorpe, Back-Pressure Compensated

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510(K) Number K802659
Device Name Flowmeter, Tube, Thorpe, Back-Pressure Compensated
Applicant DESIGN & MANUFACTURING CONSULTANTS

, US
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Regulation Number 868.2340

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Classification Product Code CAX
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Date Received 10/24/1980
Decision Date 11/12/1980
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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