The following data is part of a premarket notification filed by Liquid Crystal Products, Inc. with the FDA for Quik-temp.
| Device ID | K800666 |
| 510k Number | K800666 |
| Device Name: | QUIK-TEMP |
| Classification | Peritoneal Dialysate Filter |
| Applicant | LIQUID CRYSTAL PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPP |
| CFR Regulation Number | 876.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-03-26 |
| Decision Date | 1980-05-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() QUIK-TEMP 73354579 1229460 Dead/Cancelled |
Science Development Corporation 1982-03-15 |