Clearance Summary
GAMMA CHLOROQUINE DIPHOSPHATE SOLUTION received FDA 510(k) clearance under submission number K813342, sponsored by Gamma Biologicals, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1982-03-04.
- Submission: K813342
- Applicant / Sponsor: Gamma Biologicals, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.9400
- Decision date: 1982-03-04
Classification & Regulation
This clearance is catalogued under FDA product code KSK and 21 CFR 864.9400, within the Hematology review panel as a Class II device.