Clearance Summary
SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22) received FDA 510(k) clearance under submission number K963570, sponsored by Smiths Industries Medical Systems, Inc.. 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 1996-10-18.
- Submission: K963570
- Applicant / Sponsor: Smiths Industries Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2500
- Decision date: 1996-10-18
Classification & Regulation
This clearance is catalogued under FDA product code FMJ and 21 CFR 880.2500, within the General Hospital review panel as a Class II device.