| K-number | K891161 |
| Device name | VITRECTOMY PACK #J120 |
| Applicant | O.R. Specialties, Inc. |
| Product code | HQC |
| Device class | Class II |
| Decision date | May 26, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 886.4670 |
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