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 |