Clearance Summary
ABCO ULTRA SLIDE MICROSCOPE SLIDE received FDA 510(k) clearance under submission number K800232, sponsored by Abco Dealers, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 1980-02-21.
- Submission: K800232
- Applicant / Sponsor: Abco Dealers, Inc.
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class I
- Regulation citation: 21 CFR 864.3010
- Decision date: 1980-02-21
Classification & Regulation
This clearance is catalogued under FDA product code KEW and 21 CFR 864.3010, within the Pathology review panel as a Class I device.