The following data is part of a premarket notification filed by Cardiodynamics International Corp. with the FDA for Cardiodynamics Bioz Rx, Model 7101-sys.
| Device ID | K090602 |
| 510k Number | K090602 |
| Device Name: | CARDIODYNAMICS BIOZ RX, MODEL 7101-SYS |
| Classification | Plethysmograph, Impedance |
| Applicant | CARDIODYNAMICS INTERNATIONAL CORP. 6175 NANCY RIDGE DR., #300 San Diego, CA 92121 |
| Contact | Don Brooks |
| Correspondent | Don Brooks CARDIODYNAMICS INTERNATIONAL CORP. 6175 NANCY RIDGE DR., #300 San Diego, CA 92121 |
| Product Code | DSB |
| CFR Regulation Number | 870.2770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-03-05 |
| Decision Date | 2009-05-28 |
| Summary: | summary |