The following data is part of a premarket notification filed by Wako Pure Chemical Industries, Ltd. with the FDA for Wako Triglyceride-g Test.
Device ID | K801891 |
510k Number | K801891 |
Device Name: | WAKO TRIGLYCERIDE-G TEST |
Classification | Lipase Hydrolysis/glycerol Kinase Enzyme, Triglycerides |
Applicant | WAKO PURE CHEMICAL INDUSTRIES, LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CDT |
CFR Regulation Number | 862.1705 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-08-08 |
Decision Date | 1980-09-16 |