Clearance Summary
R & D 3K RETIC received FDA 510(k) clearance under submission number K003208, sponsored by R&D Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2000-11-07.
- Submission: K003208
- Applicant / Sponsor: R&D Systems, Inc.
- Clearance pathway: Special
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.8625
- Decision date: 2000-11-07
Classification & Regulation
This clearance is catalogued under FDA product code JPK and 21 CFR 864.8625, within the Hematology review panel as a Class II device.