Clearance Summary
PEREGRINE PIC MINIPULATOR received FDA 510(k) clearance under submission number K940392, sponsored by Peregrine Surgical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-08-23.
- Submission: K940392
- Applicant / Sponsor: Peregrine Surgical , Ltd.
- Clearance pathway: Traditional
- Review panel: Ophthalmic
- Device class: Class I
- Regulation citation: 21 CFR 886.4360
- Decision date: 1994-08-23
Classification & Regulation
This clearance is catalogued under FDA product code KYG and 21 CFR 886.4360, within the Ophthalmic review panel as a Class I device.