Clearance Summary
MULTI-PURPOSE HOLDER received FDA 510(k) clearance under submission number K884630, sponsored by Med-Dex Intl.. 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 1988-11-22.
- Submission: K884630
- Applicant / Sponsor: Med-Dex Intl.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class:
- Decision date: 1988-11-22
Classification & Regulation
This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.