Clearance Summary
PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001 received FDA 510(k) clearance under submission number K920682, sponsored by Phoenix Steri-Tech, 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 1992-04-28.
- Submission: K920682
- Applicant / Sponsor: Phoenix Steri-Tech, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4040
- Decision date: 1992-04-28
Classification & Regulation
This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.