Clearance Summary
LIFE LATCH SHARPS & BIOHAZARD CONTAINER received FDA 510(k) clearance under submission number K071088, sponsored by M&M Industries, 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 2007-07-05.
- Submission: K071088
- Applicant / Sponsor: M&M Industries, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5570
- Decision date: 2007-07-05
Classification & Regulation
This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.