Clearance Summary
MAX-I-PROBE HANDPIECE received FDA 510(k) clearance under submission number K851944, sponsored by Solo Pak Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1985-07-01.
- Submission: K851944
- Applicant / Sponsor: Solo Pak Laboratories
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4565
- Decision date: 1985-07-01
Classification & Regulation
This clearance is catalogued under FDA product code EIC and 21 CFR 872.4565, within the Dental review panel as a Class I device.