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 |