The following data is part of a premarket notification filed by Cardiometrics, Inc. with the FDA for Continuous Cardiac Output Monitoring System.
Device ID | K870150 |
510k Number | K870150 |
Device Name: | CONTINUOUS CARDIAC OUTPUT MONITORING SYSTEM |
Classification | Transducer, Ultrasonic |
Applicant | CARDIOMETRICS, INC. 645 CLYDE AVE. Mountain View, CA 94043 |
Contact | Michael J Billig |
Correspondent | Michael J Billig CARDIOMETRICS, INC. 645 CLYDE AVE. Mountain View, CA 94043 |
Product Code | JOP |
CFR Regulation Number | 870.2880 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-01-13 |
Decision Date | 1987-08-07 |