meddevicedb.com FDA Device Reference

ARTSANA PISTON AND INSULIN SYRINGES

K052667 Class II Abbreviated
Decision Date
2005-11-25
Sponsor / Applicant
Artsana S.P.A

Technical Specification

510(k) Submission ID K052667
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2005-11-25
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARTSANA PISTON AND INSULIN SYRINGES received FDA 510(k) clearance under submission number K052667, sponsored by Artsana S.P.A. 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 2005-11-25.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.