Clearance Summary
PLAXTRON SUCTION UNIT, MODEL 88AA51/88AA61 SERIES received FDA 510(k) clearance under submission number K120065, sponsored by Plaxtron Industrial (M) Sdn. Bhd.. 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 2012-04-03.
- Submission: K120065
- Applicant / Sponsor: Plaxtron Industrial (M) Sdn. Bhd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4780
- Decision date: 2012-04-03
Classification & Regulation
This clearance is catalogued under FDA product code JCX and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.