Clearance Summary
BINOCULAR MAGNIFIER 2X received FDA 510(k) clearance under submission number K830774, sponsored by Almore Intl., 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 1983-04-06.
- Submission: K830774
- Applicant / Sponsor: Almore Intl., Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5540
- Decision date: 1983-04-06
Classification & Regulation
This clearance is catalogued under FDA product code HKC and 21 CFR 886.5540, within the Ophthalmic review panel as a Class I device.