ULTRASPHYG BLOOD PRESSURE OPTION

System, Measurement, Blood-pressure, Non-invasive

CAVITRON CORP.

The following data is part of a premarket notification filed by Cavitron Corp. with the FDA for Ultrasphyg Blood Pressure Option.

Pre-market Notification Details

Device IDK780046
510k NumberK780046
Device Name:ULTRASPHYG BLOOD PRESSURE OPTION
ClassificationSystem, Measurement, Blood-pressure, Non-invasive
Applicant CAVITRON CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeDXN  
CFR Regulation Number870.1130 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-01-09
Decision Date1978-03-15

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