Clearance Summary
DISPERSALLOY-DISPERSED PHASE ALLOY SELF- received FDA 510(k) clearance under submission number K802967, sponsored by Johnson & Johnson Professionals, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1980-12-30.
- Submission: K802967
- Applicant / Sponsor: Johnson & Johnson Professionals, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.3110
- Decision date: 1980-12-30
Classification & Regulation
This clearance is catalogued under FDA product code DZS and 21 CFR 872.3110, within the Dental review panel as a Class I device.