Clearance Summary
MONOJECT STERILE 12CC SYRINGES, W/WO NEEDLES received FDA 510(k) clearance under submission number K851089, sponsored by Sherwood Medical Co.. 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 1985-04-12.
- Submission: K851089
- Applicant / Sponsor: Sherwood Medical Co.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 1985-04-12
Classification & Regulation
This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.