HORIZON 2000 PHYSIOLOGICAL PATIENT MONITOR

Computer, Blood-pressure

MENNEN MEDICAL, INC.

The following data is part of a premarket notification filed by Mennen Medical, Inc. with the FDA for Horizon 2000 Physiological Patient Monitor.

Pre-market Notification Details

Device IDK850879
510k NumberK850879
Device Name:HORIZON 2000 PHYSIOLOGICAL PATIENT MONITOR
ClassificationComputer, Blood-pressure
Applicant MENNEN MEDICAL, INC. 10123 MAIN ST. Clarence,  NY  14031
ContactRonald A Widman
CorrespondentRonald A Widman
MENNEN MEDICAL, INC. 10123 MAIN ST. Clarence,  NY  14031
Product CodeDSK  
CFR Regulation Number870.1110 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-03-04
Decision Date1985-04-25

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