meddevicedb.com FDA Device Reference

SARNS MEDICAL CART

K892052 Traditional
Decision Date
1989-06-15
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K892052
Product Code LDQ
Medical Specialty / Panel General Hospital
Decision Date 1989-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SARNS MEDICAL CART received FDA 510(k) clearance under submission number K892052, sponsored by 3M Company. 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 1989-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.