Clearance Summary
THERMAL CAUTERY UNIT, MODEL 150 received FDA 510(k) clearance under submission number K002341, sponsored by Geiger Medical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2000-10-23.
- Submission: K002341
- Applicant / Sponsor: Geiger Medical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4115
- Decision date: 2000-10-23
Classification & Regulation
This clearance is catalogued under FDA product code HQO and 21 CFR 886.4115, within the Ophthalmic review panel as a Class II device.