meddevicedb.com FDA Device Reference

MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS

K965112 Class II Traditional
Decision Date
1997-10-10
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K965112
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1997-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS received FDA 510(k) clearance under submission number K965112, sponsored by Medline Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1997-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.