Clearance Summary
DELTA-LITE CASTING TAPE & SPLINTS received FDA 510(k) clearance under submission number K802522, sponsored by Johnson & Johnson Professionals, 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 1981-01-08.
- Submission: K802522
- Applicant / Sponsor: Johnson & Johnson Professionals, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.3910
- Decision date: 1981-01-08
Classification & Regulation
This clearance is catalogued under FDA product code FYH and 21 CFR 878.3910, within the General, Plastic Surgery review panel as a Class I device.