meddevicedb.com FDA Device Reference

Halyard Sterling* Nitrile Powder-Free Exam Gloves, Halyard Sterling SG* Nitrile Sensi-Guard Powder-Free Exam Gloves

K191230 Class I Abbreviated
Decision Date
2019-11-08
Sponsor / Applicant
O&M Halyard, Inc.

Technical Specification

510(k) Submission ID K191230
Product Code LZC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2019-11-08
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Halyard Sterling* Nitrile Powder-Free Exam Gloves, Halyard Sterling SG* Nitrile Sensi-Guard Powder-Free Exam Gloves received FDA 510(k) clearance under submission number K191230, sponsored by O&M Halyard, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2019-11-08.

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.