Clearance Summary
PULSE MED CUSTOM PKG. PROC. TRAYS OPERATING ROOMS received FDA 510(k) clearance under submission number K851464, sponsored by Pulse Med, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1985-07-05.
- Submission: K851464
- Applicant / Sponsor: Pulse Med, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 1985-07-05
Classification & Regulation
This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.