PRESSURE FUNCTION BLOCK FOR BLOOD PRESS

Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm)

HONEYWELL, INC.

The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Pressure Function Block For Blood Press.

Pre-market Notification Details

Device IDK830779
510k NumberK830779
Device Name:PRESSURE FUNCTION BLOCK FOR BLOOD PRESS
ClassificationMonitor, Cardiac (incl. Cardiotachometer & Rate Alarm)
Applicant HONEYWELL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeDRT  
CFR Regulation Number870.2300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-03-11
Decision Date1983-05-09

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