Clearance Summary
DAKO MONOCLONAL MOUSE ANTI-HUMAN ESTROGEN RECEPTOR received FDA 510(k) clearance under submission number K993957, sponsored by Dako Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2000-03-03.
- Submission: K993957
- Applicant / Sponsor: Dako Corp.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.1860
- Decision date: 2000-03-03
Classification & Regulation
This clearance is catalogued under FDA product code MYA and 21 CFR 864.1860, within the Hematology review panel as a Class II device.