Clearance Summary
ONCE-A-DAY VERTOS TEST PACK received FDA 510(k) clearance under submission number K082620, sponsored by Propper Mfg. Co., Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2009-07-08.
- Submission: K082620
- Applicant / Sponsor: Propper Mfg. Co., Inc.
- Clearance pathway: Abbreviated
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2800
- Decision date: 2009-07-08
Classification & Regulation
This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.