The following data is part of a premarket notification filed by Source Production & Equipment Co., Inc. with the FDA for Spec Model M15.
| Device ID | K132969 |
| 510k Number | K132969 |
| Device Name: | SPEC MODEL M15 |
| Classification | Source, Brachytherapy, Radionuclide |
| Applicant | SOURCE PRODUCTION & EQUIPMENT CO., INC. 113 Teal St. Saint Rose, LA 70087 |
| Contact | Kelley Richardt |
| Correspondent | Kelley Richardt SOURCE PRODUCTION & EQUIPMENT CO., INC. 113 Teal St. Saint Rose, LA 70087 |
| Product Code | KXK |
| CFR Regulation Number | 892.5730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-09-23 |
| Decision Date | 2014-01-02 |
| Summary: | summary |