Clearance Summary
PERSONALLY(TM), MODEL 241 SIZES 0-12,LEFT & RIGHT received FDA 510(k) clearance under submission number K864786, sponsored by Coloplast Corp.. 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 1987-01-08.
- Submission: K864786
- Applicant / Sponsor: Coloplast Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.3800
- Decision date: 1987-01-08
Classification & Regulation
This clearance is catalogued under FDA product code GBI and 21 CFR 878.3800, within the General, Plastic Surgery review panel as a Class I device.