Clearance Summary
SYRINGE, DISPOSABLE, GLASS & PLASTIC received FDA 510(k) clearance under submission number K760005, sponsored by Stewart-Naumann Laboratories. 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 1976-08-23.
- Submission: K760005
- Applicant / Sponsor: Stewart-Naumann Laboratories
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 1976-08-23
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.