Clearance Summary
DORC INTRAOCULAR ELECTROMAGNET received FDA 510(k) clearance under submission number K830336, sponsored by Jedmed Instrument 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 1983-03-09.
- Submission: K830336
- Applicant / Sponsor: Jedmed Instrument Co.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4440
- Decision date: 1983-03-09
Classification & Regulation
This clearance is catalogued under FDA product code HPO and 21 CFR 886.4440, within the Ophthalmic review panel as a Class II device.