Clearance Summary
MODIFICATION TO STANDARD IMAGING PT 1000 ION CHAMBER received FDA 510(k) clearance under submission number K002833, sponsored by Standard Imaging, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-09-28.
- Submission: K002833
- Applicant / Sponsor: Standard Imaging, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1360
- Decision date: 2000-09-28
Classification & Regulation
This clearance is catalogued under FDA product code KPT and 21 CFR 892.1360, within the Radiology review panel as a Class II device.