510(k) K172218
K172218 is an FDA 510(k) premarket notification submitted by Mim Software, Inc. for the device "MIM Y90 Dosimetry". The FDA issued a decision of Substantially Equivalent on Nov 21, 2017. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Mim Software, Inc. has 22 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 21, 2017
- Date Received
- Jul 24, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type
- 510(k)