Clearance Summary
LUPO-TEST REGEANT received FDA 510(k) clearance under submission number K922326, sponsored by Graoipore , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1993-04-06.
- Submission: K922326
- Applicant / Sponsor: Graoipore , Ltd.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.8950
- Decision date: 1993-04-06
Classification & Regulation
This clearance is catalogued under FDA product code GIR and 21 CFR 864.8950, within the Hematology review panel as a Class I device.