Clearance Summary
NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 received FDA 510(k) clearance under submission number K013133, sponsored by Nordix, 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 2001-11-13.
- Submission: K013133
- Applicant / Sponsor: Nordix, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 2001-11-13
Classification & Regulation
This clearance is catalogued under FDA product code MOQ and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.