The following data is part of a premarket notification filed by Cas Medical Systems, Inc. with the FDA for Oscillomate Blood Pressure Monitor-model 915.
Device ID | K860488 |
510k Number | K860488 |
Device Name: | OSCILLOMATE BLOOD PRESSURE MONITOR-MODEL 915 |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | CAS MEDICAL SYSTEMS, INC. 29 BUSINESS PARK DR. Branford, CT 06405 |
Contact | Cohen, Phd |
Correspondent | Cohen, Phd CAS MEDICAL SYSTEMS, INC. 29 BUSINESS PARK DR. Branford, CT 06405 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-02-10 |
Decision Date | 1986-08-25 |