Helena Laboratories · Class I · Cleared Nov 9, 1990
| K-number | K904035 |
| Device name | REP ULTRA HDL,VLDL/LDL CHOLESTEROL SYSTEM |
| Applicant | Helena Laboratories |
| Product code | LBT |
| Device class | Class I |
| Decision date | Nov 9, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 862.1475 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov