Ophthalmic Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K042885 | OCT-OPTHALMOSCOPE | January 21, 2005 |
| K031391 | HF MODULE WITH TRANSDUCERS | June 20, 2003 |
| K030770 | OTI SCAN WITH TRANSDUCERS | March 27, 2003 |
| K024114 | A-SCAN 100 | January 10, 2003 |
| K990064 | DI-RHEX OPHTHALMIC DIATHERMY SYSTEM | April 4, 1999 |
| K974522 | 3D I-SCAN | February 25, 1998 |
| K971679 | I-SCOPE OPHTHALMIC ENDOSCOPE | June 25, 1997 |
| K960622 | I-SCAN | May 13, 1996 |
| K954263 | XE-LITE | October 18, 1995 |