The following data is part of a premarket notification filed by Cas Medical Systems, Inc. with the FDA for 740 Select.
| Device ID | K130411 | 
| 510k Number | K130411 | 
| Device Name: | 740 SELECT | 
| Classification | Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms) | 
| Applicant | CAS MEDICAL SYSTEMS, INC. 44 EAST INDUSTRIAL RD. Branford, CT 06405 | 
| Contact | Ron Jeffrey | 
| Correspondent | Ron Jeffrey CAS MEDICAL SYSTEMS, INC. 44 EAST INDUSTRIAL RD. Branford, CT 06405 | 
| Product Code | MWI | 
| CFR Regulation Number | 870.2300 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2013-02-19 | 
| Decision Date | 2013-05-29 | 
| Summary: | summary | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  740 SELECT  85832779  4539078 Live/Registered | CAS Medical Systems, Inc. 2013-01-25 |