Clearance Summary
LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES) received FDA 510(k) clearance under submission number K883980, sponsored by Menlo Care, 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 1988-12-05.
- Submission: K883980
- Applicant / Sponsor: Menlo Care, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5200
- Decision date: 1988-12-05
Classification & Regulation
This clearance is catalogued under FDA product code FOZ and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.