Clearance Summary
THE MURRAY MOBILIFT(TM) received FDA 510(k) clearance under submission number K895677, sponsored by Medical/Surgical Specialties, Ltd.. 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 1990-10-26.
- Submission: K895677
- Applicant / Sponsor: Medical/Surgical Specialties, Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5500
- Decision date: 1990-10-26
Classification & Regulation
This clearance is catalogued under FDA product code FNG and 21 CFR 880.5500, within the General Hospital review panel as a Class II device.