Clearance Summary
ANTIMICROBIAL REMOVAL DEVICE received FDA 510(k) clearance under submission number K810613, sponsored by Marion Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 1981-04-03.
- Submission: K810613
- Applicant / Sponsor: Marion Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Microbiology
- Device class: Class I
- Regulation citation: 21 CFR 866.2560
- Decision date: 1981-04-03
Classification & Regulation
This clearance is catalogued under FDA product code MDB and 21 CFR 866.2560, within the Microbiology review panel as a Class I device.