Storz Ophthalmics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K950599 | STORS SCLERAL SPONGE II (LINCOFF DESIGN) | March 2, 1995 |
| K884060 | MEDITEC QL-15 ND:YAG LASER | November 4, 1988 |