Clearance Summary
WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT received FDA 510(k) clearance under submission number K951519, sponsored by Wells Johnson Co.. 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 1995-06-14.
- Submission: K951519
- Applicant / Sponsor: Wells Johnson Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4160
- Decision date: 1995-06-14
Classification & Regulation
This clearance is catalogued under FDA product code FWL and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.