Source Production & Equipment Co., Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K162573 | Source Production & Equipment Co., Inc. Model M14 192Iridium Brachytherapy Source | November 4, 2016 |
| K161396 | SPEC Model M23 | August 17, 2016 |
| K161395 | SPEC Model M13 | July 6, 2016 |
| K150895 | SPEC Model M16 | June 19, 2015 |
| K132969 | SPEC MODEL M15 | January 2, 2014 |
| K090366 | SPEC MODEL M-31 | April 22, 2009 |
| K052947 | SOURCE PRODUCTION & EQUIPMENT CO, INC., MODEL M-19 IR-192 BRACHYTHERAPY SOURCE | April 19, 2006 |