Clearance Summary
PHILIPS RT250 COLLIMATOR (PK8050) received FDA 510(k) clearance under submission number K885126, sponsored by Perkins Mfg. Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1989-06-01.
- Submission: K885126
- Applicant / Sponsor: Perkins Mfg. Co.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5900
- Decision date: 1989-06-01
Classification & Regulation
This clearance is catalogued under FDA product code KQA and 21 CFR 892.5900, within the Radiology review panel as a Class II device.