FDA 510(k) Application Details - K062155

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

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510(K) Number K062155
Device Name Flowmeter, Tube, Thorpe, Back-Pressure Compensated
Applicant PORTER INSTRUMENT CO., INC.
49 PLAIN STREET
NORTH ATTLRBORO, MA 02760 US
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Contact CYNTHIA J.M. NOLTE
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Regulation Number 868.2340

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Classification Product Code CAX
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Date Received 07/28/2006
Decision Date 11/09/2006
Decision SESE - SUBST EQUIV
Classification Advisory Committee AN - Anesthesiology
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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