Clearance Summary
MANAN EPIDURAL NEEDLE received FDA 510(k) clearance under submission number K852428, sponsored by Manan Manufacturing Co., 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 1985-06-27.
- Submission: K852428
- Applicant / Sponsor: Manan Manufacturing Co., Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4200
- Decision date: 1985-06-27
Classification & Regulation
This clearance is catalogued under FDA product code GCB and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.