Clearance Summary
DR.500O OPERATING TABLE received FDA 510(k) clearance under submission number K864295, sponsored by Koken Mfg Company, 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 1986-11-19.
- Submission: K864295
- Applicant / Sponsor: Koken Mfg Company, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4960
- Decision date: 1986-11-19
Classification & Regulation
This clearance is catalogued under FDA product code FQO and 21 CFR 878.4960, within the General, Plastic Surgery review panel as a Class I device.