The following data is part of a premarket notification filed by Data Medical Associates, Inc. with the FDA for Hdl Cholesterol Precipitating Procedure.
Device ID | K881326 |
510k Number | K881326 |
Device Name: | HDL CHOLESTEROL PRECIPITATING PROCEDURE |
Classification | Ldl & Vldl Precipitation, Hdl |
Applicant | DATA MEDICAL ASSOCIATES, INC. 845 AVENUE G EAST Arlington, TX 76011 |
Contact | Marjorie B Potts |
Correspondent | Marjorie B Potts DATA MEDICAL ASSOCIATES, INC. 845 AVENUE G EAST Arlington, TX 76011 |
Product Code | LBR |
CFR Regulation Number | 862.1475 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-03-29 |
Decision Date | 1988-05-27 |