Clearance Summary
L(3), LYSNIG LEAD LATEX RADIATION GLOVE(R) received FDA 510(k) clearance under submission number K896076, sponsored by Advance Medical Designs, 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 1990-01-04.
- Submission: K896076
- Applicant / Sponsor: Advance Medical Designs, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6250
- Decision date: 1990-01-04
Classification & Regulation
This clearance is catalogued under FDA product code LZC and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.