Seiko Optical Products of America, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K942513 | SEIKO EYEGLASS FRAME | July 15, 1994 |
| K900764 | SUNGLASS, NON-PRESCRIPTION | June 20, 1990 |
| K873245 | AR DIACOAT SINGLE VISION LENSES | October 5, 1987 |
| K861684 | SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS) | June 9, 1986 |