Clearance Summary
MICROCAP received FDA 510(k) clearance under submission number K981114, sponsored by Oridion Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1998-06-25.
- Submission: K981114
- Applicant / Sponsor: Oridion Medical , Ltd.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 1998-06-25
Classification & Regulation
This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.