The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Boehringer Mannheim Direct Ldl - Cholesterol.
| Device ID | K974733 |
| 510k Number | K974733 |
| Device Name: | BOEHRINGER MANNHEIM DIRECT LDL - CHOLESTEROL |
| Classification | Ldl & Vldl Precipitation, Hdl |
| Applicant | BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Contact | Edward R Kimmelman |
| Correspondent | Edward R Kimmelman BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Product Code | LBR |
| CFR Regulation Number | 862.1475 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-12-18 |
| Decision Date | 1998-01-26 |
| Summary: | summary |