510(k) K890799
K890799 is an FDA 510(k) premarket notification submitted by Cis-Us, Inc. for the device "CURIETRON 192 HIGH DOSE RATE". The FDA issued a decision of Substantially Equivalent on October 27, 1989. The device falls under product code JAQ (System, Applicator, Radionuclide, Remote-Controlled), a Class II device regulated under 21 CFR 892.5700. Cis-Us, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 27, 1989
- Date Received
- February 17, 1989
- 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