The following data is part of a premarket notification filed by Medex, Inc. with the FDA for Microflush.
Device ID | K790455 |
510k Number | K790455 |
Device Name: | MICROFLUSH |
Classification | Catheter, Continuous Flush |
Applicant | MEDEX, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KRA |
CFR Regulation Number | 870.1210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-03-05 |
Decision Date | 1979-03-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MICROFLUSH 75553038 2325638 Live/Registered |
CLEAN HARBORS INDUSTRIAL SERVICES, INC. 1998-09-14 |
![]() MICROFLUSH 73446890 1292119 Live/Registered |
Microphor, Inc. 1983-10-06 |