Clearance Summary
CLINITEX VIS-X ASPIRATING ACCESSORY received FDA 510(k) clearance under submission number K780852, sponsored by Varian Assoc., 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 1978-11-03.
- Submission: K780852
- Applicant / Sponsor: Varian Assoc., Inc.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.4150
- Decision date: 1978-11-03
Classification & Regulation
This clearance is catalogued under FDA product code HKP and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.