Clearance Summary
NORMLCERA received FDA 510(k) clearance under submission number K810268, sponsored by Medical Specialties Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1981-03-06.
- Submission: K810268
- Applicant / Sponsor: Medical Specialties Laboratories
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class I
- Regulation citation: 21 CFR 864.2800
- Decision date: 1981-03-06
Classification & Regulation
This clearance is catalogued under FDA product code KIS and 21 CFR 864.2800, within the Hematology review panel as a Class I device.