Clearance Summary
Delta 3300 received FDA 510(k) clearance under submission number K190437, sponsored by Netech Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-08-28.
- Submission: K190437
- Applicant / Sponsor: Netech Corporation
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5325
- Decision date: 2019-08-28
Classification & Regulation
This clearance is catalogued under FDA product code DRL and 21 CFR 870.5325, within the Cardiovascular review panel as a Class II device.