Clearance Summary
CRYO CHECK FACTOR VII DEFICIENT PLASMA received FDA 510(k) clearance under submission number K971224, sponsored by Precision 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 1997-07-17.
- Submission: K971224
- Applicant / Sponsor: Precision Biologicals, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7290
- Decision date: 1997-07-17
Classification & Regulation
This clearance is catalogued under FDA product code GJT and 21 CFR 864.7290, within the Hematology review panel as a Class II device.