SIMPLICITY PLUS
Pump, Infusion
CRITIKON COMPANY,LLC
The following data is part of a premarket notification filed by Critikon Company,llc with the FDA for Simplicity Plus.
Pre-market Notification Details
| Device ID | K831761 |
| 510k Number | K831761 |
| Device Name: | SIMPLICITY PLUS |
| Classification | Pump, Infusion |
| Applicant | CRITIKON COMPANY,LLC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FRN |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-06-01 |
| Decision Date | 1983-08-12 |
Trademark Results [SIMPLICITY PLUS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SIMPLICITY PLUS 85650965 4590991 Live/Registered |
NORMERICA INTERNATIONAL CORPORATION 2012-06-13 |
 SIMPLICITY PLUS 75096632 not registered Dead/Abandoned |
Eatonform, Inc. 1996-04-29 |
 SIMPLICITY PLUS 74436540 1891377 Dead/Cancelled |
NYNEX Corporation 1993-09-17 |
 SIMPLICITY PLUS 74385755 not registered Dead/Abandoned |
Quies Corp. 1993-05-03 |
 SIMPLICITY PLUS 74218432 1856381 Dead/Cancelled |
Normerica Inc. 1991-11-04 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.