510(k) K150895
K150895 is an FDA 510(k) premarket notification submitted by Source Production and Equipment Co., Inc. for the device "SPEC Model M16". The FDA issued a decision of Substantially Equivalent on June 19, 2015. The device falls under product code KXK (Source, Brachytherapy, Radionuclide), a Class II device regulated under 21 CFR 892.5730. Source Production and Equipment Co., Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 19, 2015
- Date Received
- April 2, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Source, Brachytherapy, Radionuclide
- Device Class
- Class II
- Regulation Number
- 892.5730
- Review Panel
- RA
- Submission Type