Clearance Summary
STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) received FDA 510(k) clearance under submission number K040300, sponsored by Stryker Instruments. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2004-03-03.
- Submission: K040300
- Applicant / Sponsor: Stryker Instruments
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4250
- Decision date: 2004-03-03
Classification & Regulation
This clearance is catalogued under FDA product code ERL and 21 CFR 874.4250, within the Ear, Nose, Throat review panel as a Class II device.