510(k) K954679
K954679 is an FDA 510(k) premarket notification submitted by Theratronics, Inc. for the device "THERAPLAN PLUS". The FDA issued a decision of Substantially Equivalent on November 8, 1996. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. Theratronics, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 8, 1996
- Date Received
- October 10, 1995
- 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