Clearance Summary
EFFNER CAUTERY INSTRUMENTS received FDA 510(k) clearance under submission number K875260, sponsored by Effner and Spreine Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1988-06-06.
- Submission: K875260
- Applicant / Sponsor: Effner and Spreine Co.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4115
- Decision date: 1988-06-06
Classification & Regulation
This clearance is catalogued under FDA product code HQP and 21 CFR 886.4115, within the Ophthalmic review panel as a Class II device.