Clearance Summary
REAGENTS FOR USE ON CONTRAVES DC300, DC500, AL801 received FDA 510(k) clearance under submission number K873832, sponsored by In Vitro Diagnostics, 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 1987-11-23.
- Submission: K873832
- Applicant / Sponsor: In Vitro Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.8165
- Decision date: 1987-11-23
Classification & Regulation
This clearance is catalogued under FDA product code KRZ and 21 CFR 864.8165, within the Hematology review panel as a Class II device.