Clearance Summary
TERATECH MODEL 10V5 SMART PROBE received FDA 510(k) clearance under submission number K040840, sponsored by Teratech Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2004-04-14.
- Submission: K040840
- Applicant / Sponsor: Teratech Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1570
- Decision date: 2004-04-14
Classification & Regulation
This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.