The following data is part of a premarket notification filed by Creative Laboratory Products, Inc. with the FDA for High Density Lipoprotein Cholesterol.
Device ID | K912823 |
510k Number | K912823 |
Device Name: | HIGH DENSITY LIPOPROTEIN CHOLESTEROL |
Classification | Ldl & Vldl Precipitation, Hdl |
Applicant | CREATIVE LABORATORY PRODUCTS, INC. 6258 LA PAS TRAIL Indianapolis, IN 46268 |
Contact | Gary J Proksch |
Correspondent | Gary J Proksch CREATIVE LABORATORY PRODUCTS, INC. 6258 LA PAS TRAIL Indianapolis, IN 46268 |
Product Code | LBR |
CFR Regulation Number | 862.1475 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-06-26 |
Decision Date | 1991-08-16 |