510(k) K150265
K150265 is an FDA 510(k) premarket notification submitted by Cnmc Company Incorporated for the device "Model 206 Electrometer/Dosimeter". The FDA issued a decision of Substantially Equivalent on Sep 3, 2015. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 3, 2015
- Date Received
- Feb 4, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accelerator, Linear, Medical
- Device Class
- Class II
- Regulation Number
- 892.5050
- Review Panel
- RA
- Submission Type
- 510(k)