| K-number | K890992 |
| Device name | WOODLYN OPHTHALMIC PROJECTOR |
| Applicant | Woodlyn, Inc. |
| Product code | HOS |
| Device class | Class I |
| Decision date | May 17, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 886.1680 |
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