Clearance Summary
NULIFE received FDA 510(k) clearance under submission number K955055, sponsored by Med-Tech Rubber & Engineering Industries. 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 1996-01-23.
- Submission: K955055
- Applicant / Sponsor: Med-Tech Rubber & Engineering Industries
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1996-01-23
Classification & Regulation
This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.