510(k) K802243
K802243 is an FDA 510(k) premarket notification submitted by Progress Mankind Technology for the device "VAXIOM FAMILY OF RF LESION PROBES & ELEC". The FDA issued a decision of Substantially Equivalent on November 12, 1980. The device falls under product code GXI (Probe, Radiofrequency Lesion), a Class II device regulated under 21 CFR 882.4725. Progress Mankind Technology has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 12, 1980
- Date Received
- September 16, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Probe, Radiofrequency Lesion
- Device Class
- Class II
- Regulation Number
- 882.4725
- Review Panel
- NE
- Submission Type