Clearance Summary
VITALMAX 2100/2200 received FDA 510(k) clearance under submission number K905274, sponsored by Pace Tech, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-07-17.
- Submission: K905274
- Applicant / Sponsor: Pace Tech, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 1991-07-17
Classification & Regulation
This clearance is catalogued under FDA product code DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.