Coburn Optical Ind., Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K892351 | MAGNILINK SYSTEM 602 | May 26, 1989 |
| K892348 | MAGNILINK SYSTEM 201 | May 26, 1989 |
| K892350 | MAGNILINK SYSTEM 402/5 | May 26, 1989 |
| K892349 | MAGNILINK SYSTEM 209 | May 26, 1989 |
| K892347 | MAGNILINK SYSTEM 101 | May 26, 1989 |
| K862188 | IRRIGATION & ASPIRATION/VITRECTOMY DEVICE | August 21, 1986 |
| K853457 | COBURN I/A SYSTEM | October 15, 1985 |
| K821737 | DISP. MICROSURGICAL KNIVES | July 2, 1982 |
| K812441 | DI-CROWN | October 6, 1981 |
| K803159 | AUTOMATED PERIMETERS | February 4, 1981 |
| K801659 | BIOPHTAL CLINICAL ENDOTHELIAL MICROSCOPE | September 9, 1980 |
| K801231 | EYE-VAC | July 21, 1980 |
| K791659 | MEDITEC (RODENSTOCK) LASER PHOTOCOAGUL | October 11, 1979 |
| K781507 | RETINOMETER | November 15, 1978 |