Clearance Summary
SUTURE REMOVAL KIT received FDA 510(k) clearance under submission number K803199, sponsored by Walpak 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 1981-01-15.
- Submission: K803199
- Applicant / Sponsor: Walpak Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1981-01-15
Classification & Regulation
This clearance is catalogued under FDA product code KDD and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.