Clearance Summary
AMERITEK SURE-POINT HDR NEEDLE TEMPLATE received FDA 510(k) clearance under submission number K031273, sponsored by Amertek Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-07-15.
- Submission: K031273
- Applicant / Sponsor: Amertek Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5700
- Decision date: 2003-07-15
Classification & Regulation
This clearance is catalogued under FDA product code JAQ and 21 CFR 892.5700, within the Radiology review panel as a Class II device.