Clearance Summary
NEEDLE & BLADE COUNTER & DISPOSAL UNIT received FDA 510(k) clearance under submission number K872313, sponsored by Gary Plastic Packaging 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 1987-07-02.
- Submission: K872313
- Applicant / Sponsor: Gary Plastic Packaging Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5570
- Decision date: 1987-07-02
Classification & Regulation
This clearance is catalogued under FDA product code MMK and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.