Clearance Summary
PRIMA ANAESTHESIA MACHINE received FDA 510(k) clearance under submission number K061102, sponsored by Penlon , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2006-07-28.
- Submission: K061102
- Applicant / Sponsor: Penlon , Ltd.
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5160
- Decision date: 2006-07-28
Classification & Regulation
This clearance is catalogued under FDA product code BSZ and 21 CFR 868.5160, within the Anesthesiology review panel as a Class II device.