Clearance Summary
DERMALON,SURGILON,OPHTHALON,& OPHTHALMIC NYLON SUT received FDA 510(k) clearance under submission number K930586, sponsored by Davis & Geck, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1993-12-17.
- Submission: K930586
- Applicant / Sponsor: Davis & Geck, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.5020
- Decision date: 1993-12-17
Classification & Regulation
This clearance is catalogued under FDA product code GAR and 21 CFR 878.5020, within the General, Plastic Surgery review panel as a Class II device.