The following data is part of a premarket notification filed by Roche Diagnostics Corp. with the FDA for Hdl Cholesterol Plus.
| Device ID | K000568 |
| 510k Number | K000568 |
| Device Name: | HDL CHOLESTEROL PLUS |
| Classification | Electrophoresis, Cholesterol Via Esterase-oxidase, Hdl |
| Applicant | ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. P.O. BOX 50457 Indianapolis, IN 46250 -0457 |
| Contact | Kay A Taylor |
| Correspondent | Kay A Taylor ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. P.O. BOX 50457 Indianapolis, IN 46250 -0457 |
| Product Code | LBT |
| CFR Regulation Number | 862.1475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-02-22 |
| Decision Date | 2000-08-04 |