| K-number | K894544 |
| Device name | BIOTROL RUB-E.I.A. TEST G |
| Applicant | Biotrol, USA, Inc. |
| Product code | LFX |
| Device class | Class II |
| Decision date | Aug 30, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 866.3510 |
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