Clearance Summary
MODEL 7410 VOYAGER received FDA 510(k) clearance under submission number K974879, sponsored by Healthdyne Technologies, 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 1998-06-29.
- Submission: K974879
- Applicant / Sponsor: Healthdyne Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 1998-06-29
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.