CELL-CHEX
Mixture, Hematology Quality Control
STRECK LABORATORIES, INC.
The following data is part of a premarket notification filed by Streck Laboratories, Inc. with the FDA for Cell-chex.
Pre-market Notification Details
| Device ID | K780140 |
| 510k Number | K780140 |
| Device Name: | CELL-CHEX |
| Classification | Mixture, Hematology Quality Control |
| Applicant | STRECK LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JPK |
| CFR Regulation Number | 864.8625 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-01-26 |
| Decision Date | 1978-03-27 |
Trademark Results [CELL-CHEX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CELL-CHEX 85410938 4166939 Live/Registered |
Streck, Inc. 2011-08-30 |
 CELL-CHEX 78700736 not registered Dead/Abandoned |
Streck Laboratories, Inc. 2005-08-25 |
 CELL-CHEX 77818922 not registered Dead/Abandoned |
Streck, Inc. 2009-09-02 |
 CELL-CHEX 73024278 1027707 Dead/Expired |
STRECK LABORATORIES, INC. 1974-06-14 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.