Clearance Summary
ARSOFT received FDA 510(k) clearance under submission number K983146, sponsored by Alliance Rubber Products Sdn. Bhd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1998-12-07.
- Submission: K983146
- Applicant / Sponsor: Alliance Rubber Products Sdn. Bhd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1998-12-07
Classification & Regulation
This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.