Clearance Summary
DEVILBISS MODEL 7352 SERIES received FDA 510(k) clearance under submission number K904766, sponsored by Devilbiss Health Care, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1991-03-26.
- Submission: K904766
- Applicant / Sponsor: Devilbiss Health Care, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 1991-03-26
Classification & Regulation
This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.