740 SELECT

Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms)

CAS MEDICAL SYSTEMS, INC.

The following data is part of a premarket notification filed by Cas Medical Systems, Inc. with the FDA for 740 Select.

Pre-market Notification Details

Device IDK150620
510k NumberK150620
Device Name:740 SELECT
ClassificationMonitor, Physiological, Patient (without Arrhythmia Detection Or Alarms)
Applicant CAS MEDICAL SYSTEMS, INC. 44 EAST INDUSTRIAL RD. Branford,  CT  06405
ContactRon Jeffrey
CorrespondentRon Jeffrey
CAS MEDICAL SYSTEMS, INC. 44 EAST INDUSTRIAL RD. Branford,  CT  06405
Product CodeMWI  
CFR Regulation Number870.2300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2015-03-10
Decision Date2015-05-08
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00851920007293 K150620 000
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00851920007125 K150620 000
00851920007118 K150620 000
00851920007101 K150620 000
00851920007446 K150620 000

Trademark Results [740 SELECT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
740 SELECT
740 SELECT
85832779 4539078 Live/Registered
CAS Medical Systems, Inc.
2013-01-25

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