510(k) K193240
K193240 is an FDA 510(k) premarket notification submitted by Varian Medical Systems, Inc. for the device "Universal Cylinder Applicator Family". The FDA issued a decision of Substantially Equivalent on Aug 17, 2020. The device falls under product code JAQ (System, Applicator, Radionuclide, Remote-Controlled), a Class II device regulated under 21 CFR 892.5700. Varian Medical Systems, Inc. has 205 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 17, 2020
- Date Received
- Nov 25, 2019
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Applicator, Radionuclide, Remote-Controlled
- Device Class
- Class II
- Regulation Number
- 892.5700
- Review Panel
- RA
- Submission Type
- 510(k)