Storz Instrument Co. · Class II · Cleared Mar 30, 1992
| K-number | K921106 |
| Device name | STERILE/SINGLE USE EYE SPHERE IMPLANTS |
| Applicant | Storz Instrument Co. |
| Product code | HPZ |
| Device class | Class II |
| Decision date | Mar 30, 1992 |
| Decision | Substantially Equivalent |
| Regulation | 886.3320 |
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