Clearance Summary
INTRACAVITARY MOULD APPLICATOR SET, MODEL 189.001 received FDA 510(k) clearance under submission number K041715, sponsored by Nucletron 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 2005-03-24.
- Submission: K041715
- Applicant / Sponsor: Nucletron Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5700
- Decision date: 2005-03-24
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.