Clearance Summary
A+MED DISPOSABLE NEEDLE received FDA 510(k) clearance under submission number K870193, sponsored by Can-Am Surgical Corp.. 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 1987-02-27.
- Submission: K870193
- Applicant / Sponsor: Can-Am Surgical Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5570
- Decision date: 1987-02-27
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.