Clearance Summary
SMARTLOCK SAFETY SYRINGE received FDA 510(k) clearance under submission number K973888, sponsored by Medical Innovation , 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 1998-06-03.
- Submission: K973888
- Applicant / Sponsor: Medical Innovation , Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 1998-06-03
Classification & Regulation
This clearance is catalogued under FDA product code MEG and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.