| K-number | K940997 |
| Device name | AL-3300 |
| Applicant | Hoya Corp. USA |
| Product code | HLM |
| Device class | Class I |
| Decision date | Sep 29, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 886.1425 |
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