Clearance Summary
RNG SERIES ULTRASOUND NEEDLE/CATH. GDS received FDA 510(k) clearance under submission number K820269, sponsored by CIVCO Medical Instruments 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 1982-03-23.
- Submission: K820269
- Applicant / Sponsor: CIVCO Medical Instruments Co., Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1982-03-23
Classification & Regulation
This clearance is catalogued under FDA product code DWO and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.