510(k) K900434
K900434 is an FDA 510(k) premarket notification submitted by Scanditronix, Inc. for the device "MM-22 MICROTRON, MM50 MICROTRON". The FDA issued a decision of Substantially Equivalent on October 23, 1990. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Scanditronix, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 23, 1990
- Date Received
- January 30, 1990
- 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