Clearance Summary
P.O.P. PAIN KIT received FDA 510(k) clearance under submission number K001342, sponsored by Post Operative Pain Management. 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 2000-09-07.
- Submission: K001342
- Applicant / Sponsor: Post Operative Pain Management
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5725
- Decision date: 2000-09-07
Classification & Regulation
This clearance is catalogued under FDA product code MEB and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.