Clearance Summary
DISPOSABLE CIRCULAR STAPLER, MODELS WHY-25, WHY-29. WHY 32 received FDA 510(k) clearance under submission number K100386, sponsored by Changzhou Waston Medical Appliance Co., Ltd.. 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 2010-03-01.
- Submission: K100386
- Applicant / Sponsor: Changzhou Waston Medical Appliance Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4750
- Decision date: 2010-03-01
Classification & Regulation
This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.