Burton Medical Products Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 15
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K101537 | AIM 200, MAJOR SURGICAL LIGHT | September 30, 2010 |
| K042395 | OUTPATIENT III MINOR SURGERY LIGHT | December 1, 2004 |
| K000639 | VISIONARY 2000 | May 25, 2000 |
| K963682 | GENIE' SINGLE CEILING AND DOUBLE CEILING | November 13, 1996 |
| K961843 | GENIE | August 22, 1996 |
| K935102 | SATURN LIGHT | June 27, 1994 |
| K942553 | GENESIS | June 23, 1994 |
| K936088 | WAVE FLUORESCENT MAGNIFIER | April 26, 1994 |
| K931645 | HALUX TASKLIGHT | August 20, 1993 |
| K901706 | LIGHT, HEAD, EXAMINATION | July 19, 1990 |
| K893807 | MODEL 0183010, PEARL MEDICAL EXAM LIGHT | August 15, 1989 |
| K893808 | MODEL 0450000, OPAL MEDICAL EXAM LIGHT | August 15, 1989 |
| K861289 | BASIC LIGHT | April 18, 1986 |
| K860088 | PL EXAM LIGHT | January 24, 1986 |
| K851742 | MEDICAL EXAMINATION LIGHTS | May 13, 1985 |