The following data is part of a premarket notification filed by Dynatech Research & Development Co. with the FDA for Chest Fluid Monitor.
| Device ID | K772092 |
| 510k Number | K772092 |
| Device Name: | CHEST FLUID MONITOR |
| Classification | Plethysmograph, Impedance |
| Applicant | DYNATECH RESEARCH & DEVELOPMENT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DSB |
| CFR Regulation Number | 870.2770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-11-07 |
| Decision Date | 1977-11-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CHEST FLUID MONITOR 77744834 not registered Dead/Abandoned |
Singer, Michaeal George 2009-05-26 |