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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name analyzer, gas, oxygen, gaseous-phase
510(k) Number K883254
Device Name MULTINEX MONITOR (MODIFICATION)
Applicant
DATASCOPE CORP.
WINTERS AVE.
P.O. BOX 5
PARAMUS,  NJ  07653 -0005
Applicant Contact ARTHUR FRIEDMAN
Correspondent
DATASCOPE CORP.
WINTERS AVE.
P.O. BOX 5
PARAMUS,  NJ  07653 -0005
Correspondent Contact ARTHUR FRIEDMAN
Regulation Number868.1720
Classification Product Code
CCL  
Date Received08/02/1988
Decision Date 09/12/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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