Clearance Summary
AEF POSIDYNE I.V. FILTER/AIR ELIMINATOR received FDA 510(k) clearance under submission number K850825, sponsored by Pall Biomedical Products Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1985-04-09.
- Submission: K850825
- Applicant / Sponsor: Pall Biomedical Products Co.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 1985-04-09
Classification & Regulation
This clearance is catalogued under FDA product code FPB and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.