Clearance Summary
FLOW=MED received FDA 510(k) clearance under submission number K924322, sponsored by International Electronic Technology Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1994-04-26.
- Submission: K924322
- Applicant / Sponsor: International Electronic Technology Corp.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1860
- Decision date: 1994-04-26
Classification & Regulation
This clearance is catalogued under FDA product code BZH and 21 CFR 868.1860, within the Anesthesiology review panel as a Class II device.