Clearance Summary
CONTACT LENS REMOVER AND INSERTER received FDA 510(k) clearance under submission number K780663, sponsored by Dmv Contact Lens 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 1978-05-17.
- Submission: K780663
- Applicant / Sponsor: Dmv Contact Lens Co.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.5420
- Decision date: 1978-05-17
Classification & Regulation
This clearance is catalogued under FDA product code KYE and 21 CFR 886.5420, within the Ophthalmic review panel as a Class I device.